A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12878777



Internal ID2171887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:86666303..86676756hg38UCSC Ensembl
Innerchr7:86666316..86676744hg38UCSC Ensembl
Outerchr7:86666291..86676769hg38UCSC Ensembl
chr7:86295619..86306072hg19UCSC Ensembl
Innerchr7:86295632..86306060hg19UCSC Ensembl
Outerchr7:86295607..86306085hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3810454
hg1910454
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3614018
Supporting Variants
SamplesHG01961
Known GenesGRM3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12878777
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer