A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698483



Internal ID15435135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:135661977..135680889hg38UCSC Ensembl
Innerchr6:135983115..136002027hg19UCSC Ensembl
Innerchr6:136024808..136043720hg18UCSC Ensembl
Innerchr6:136024808..136043720hg17UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3818913
hg1918913
hg1818913
hg1718913
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522833
Supporting Variants
Samples
Known GenesLINC00271, MIR548H4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698483
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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