A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3613964



Internal ID7000859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:84301051..84453488hg38UCSC Ensembl
Innerchr7:84301051..84453488hg38UCSC Ensembl
Outerchr7:84300551..84453988hg38UCSC Ensembl
chr7:83930367..84082804hg19UCSC Ensembl
Innerchr7:83930367..84082804hg19UCSC Ensembl
Outerchr7:83929867..84083304hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38152438
hg19152438
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12875155
SamplesHG04054
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3613964
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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