A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12857800



Internal ID2859616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:77310267..77317343hg38UCSC Ensembl
Innerchr7:77310767..77316843hg38UCSC Ensembl
Outerchr7:77309267..77318343hg38UCSC Ensembl
chr7:76939584..76946660hg19UCSC Ensembl
Innerchr7:76940084..76946160hg19UCSC Ensembl
Outerchr7:76938584..76947660hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg387077
hg197077
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3613797
Supporting Variants
SamplesHG01488
Known GenesGSAP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12857800
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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