A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625925



Internal ID7012759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35223947..35236404hg38UCSC Ensembl
chr11:35245494..35257951hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3812458
hg1912458
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14090155, essv14090165, essv14090156, essv14090159, essv14090178, essv14090163, essv14090175, essv14090167, essv14090176, essv14090164, essv14090162, essv14090160, essv14090168, essv14090158, essv14090172, essv14090174, essv14090161, essv14090169, essv14090166, essv14090173, essv14090170, essv14090171, essv14090177, essv14090157
SamplesHG00650, HG00524, HG02375, HG02061, HG01802, HG00599, HG01848, HG02067, HG02082, HG02138, HG00406, HG00530, HG00475, HG02084, HG01029, HG00690, HG02048, HG01596, HG01812, HG00625, HG01598, HG02396, HG01817, HG01869
Known GenesCD44
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625925
Frequency
Sample Size2504
Observed Gain24
Observed Loss0
Observed Complex0
Frequencyn/a


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