A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv693300



Internal ID15429952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:85836405..85856225hg38UCSC Ensembl
Innerchr6:86546123..86565943hg19UCSC Ensembl
Innerchr6:86602842..86622662hg18UCSC Ensembl
Innerchr6:86602842..86622662hg17UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3819821
hg1919821
hg1819821
hg1719821
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515896
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv693300
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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