A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv684748



Internal ID15074714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:113356672..113382693hg38UCSC Ensembl
Innerchr9:116118952..116144973hg19UCSC Ensembl
Innerchr9:115158773..115184794hg18UCSC Ensembl
Innerchr9:113198506..113224527hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3826022
hg1926022
hg1826022
hg1726022
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519849
Supporting Variants
Samples
Known GenesBSPRY, HDHD3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv684748
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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