A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624952



Internal ID7011802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:131110819..131114518hg38UCSC Ensembl
chr10:132909082..132912781hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg383700
hg193700
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13976873, essv13976870, essv13976871, essv13976869, essv13976872, essv13976867, essv13976868, essv13976874
SamplesHG02339, HG01971, HG03490, HG02603, HG03862, HG03711, HG04025, HG03642
Known GenesTCERG1L
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624952
Frequency
Sample Size2504
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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