A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12877073



Internal ID4552198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:85346400..85379307hg38UCSC Ensembl
Innerchr7:85346400..85379307hg38UCSC Ensembl
Outerchr7:85345900..85379807hg38UCSC Ensembl
chr7:84975716..85008623hg19UCSC Ensembl
Innerchr7:84975716..85008623hg19UCSC Ensembl
Outerchr7:84975216..85009123hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3832908
hg1932908
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3613989
Supporting Variants
SamplesHG04054
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12877073
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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