A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12901105



Internal ID2902921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:96487069..96488089hg38UCSC Ensembl
Innerchr7:96487069..96488089hg38UCSC Ensembl
Outerchr7:96487069..96488089hg38UCSC Ensembl
chr7:96116381..96117401hg19UCSC Ensembl
Innerchr7:96116381..96117401hg19UCSC Ensembl
Outerchr7:96116381..96117401hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg381021
hg191021
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3614213
Supporting Variants
SamplesNA18498
Known GenesC7orf76
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12901105
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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