A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694888



Internal ID15431540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:3028893..3044653hg38UCSC Ensembl
Innerchr6:3029127..3044887hg19UCSC Ensembl
Innerchr6:2974126..2989886hg18UCSC Ensembl
Innerchr6:2974126..2989886hg17UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg3815761
hg1915761
hg1815761
hg1715761
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522115
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694888
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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