A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3607938



Internal ID6994869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3924204..3925986hg38UCSC Ensembl
Innerchr6:3924204..3925986hg38UCSC Ensembl
Outerchr6:3924004..3926188hg38UCSC Ensembl
chr6:3924438..3926220hg19UCSC Ensembl
Innerchr6:3924438..3926220hg19UCSC Ensembl
Outerchr6:3924238..3926422hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg381783
hg191783
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12179399, essv12179397, essv12179402, essv12179398, essv12179400, essv12179401
SamplesHG00881, HG03100, HG00458, HG00844, NA18945, HG02139
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3607938
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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