A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634934



Internal ID7021734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:74104411..74129935hg38UCSC Ensembl
chr14:74571114..74596638hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3825525
hg1925525
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15061095, essv15061082, essv15061096, essv15061079, essv15061081, essv15061078, essv15061091, essv15061076, essv15061077, essv15061080, essv15061090, essv15061097, essv15061087, essv15061093, essv15061084, essv15061083, essv15061092, essv15061089, essv15061085, essv15061094, essv15061088, essv15061086
SamplesNA19701, NA19914, NA18504, HG03295, HG03082, HG02621, NA19319, HG02485, HG02541, NA18498, HG03055, HG03120, NA18933, HG02511, NA19455, NA18907, NA19449, HG02675, HG01363, HG02010, HG01912, HG03129
Known GenesLIN52
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634934
Frequency
Sample Size2504
Observed Gain22
Observed Loss0
Observed Complex0
Frequencyn/a


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