A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698035



Internal ID15088001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:93157826..93161911hg38UCSC Ensembl
Innerchr6:93867544..93871629hg19UCSC Ensembl
Innerchr6:93924265..93928350hg18UCSC Ensembl
Innerchr6:93924265..93928350hg17UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg384086
hg194086
hg184086
hg174086
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517329
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698035
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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