A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3632503



Internal ID6672627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:66317472..66327540hg38UCSC Ensembl
chr13:66891604..66901672hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3810069
hg1910069
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14777471, essv14777460, essv14777475, essv14777464, essv14777458, essv14777478, essv14777459, essv14777470, essv14777477, essv14777468, essv14777462, essv14777480, essv14777473, essv14777476, essv14777479, essv14777482, essv14777465, essv14777461, essv14777469, essv14777474, essv14777481, essv14777472, essv14777463, essv14777466, essv14777467
SamplesHG03130, HG03521, HG03577, NA19107, HG03572, HG02621, HG03091, NA19719, HG01950, NA18908, HG02442, HG03291, HG02953, HG03123, NA18879, HG03476, HG01988, HG00128, HG02557, HG03419, HG03063, HG03410, HG03401, HG02284, HG02343
Known GenesPCDH9
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3632503
Frequency
Sample Size2504
Observed Gain0
Observed Loss25
Observed Complex0
Frequencyn/a


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