A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636295



Internal ID6676404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43629021..43655523hg38UCSC Ensembl
chr15:43921219..43947721hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg3826503
hg1926503
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15231470, essv15231459, essv15231468, essv15231482, essv15231472, essv15231484, essv15231461, essv15231462, essv15231467, essv15231471, essv15231457, essv15231487, essv15231477, essv15231460, essv15231485, essv15231456, essv15231486, essv15231465, essv15231463, essv15231474, essv15231483, essv15231469, essv15231475, essv15231481, essv15231478, essv15231480, essv15231476, essv15231466, essv15231464, essv15231458, essv15231479, essv15231473
SamplesHG02614, HG01054, HG01031, HG03772, HG02040, HG02407, NA18993, HG03040, NA18964, HG02981, HG02562, NA19383, HG01121, NA18640, HG03114, HG01353, HG01183, HG04062, HG01790, HG01612, HG02014, HG03046, HG04159, HG03354, HG00246, HG03109, HG01812, HG01974, HG04080, NA18971, NA18873, NA20503
Known GenesCATSPER2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636295
Frequency
Sample Size2504
Observed Gain32
Observed Loss0
Observed Complex0
Frequencyn/a


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