A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3613881



Internal ID7000776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:81154085..81156703hg38UCSC Ensembl
Innerchr7:81154101..81156688hg38UCSC Ensembl
Outerchr7:81154070..81156719hg38UCSC Ensembl
chr7:80783401..80786019hg19UCSC Ensembl
Innerchr7:80783417..80786004hg19UCSC Ensembl
Outerchr7:80783386..80786035hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg382619
hg192619
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12864800, essv12864801, essv12864799
SamplesHG03646, HG03733, HG02774
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3613881
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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