A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695601



Internal ID15085567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:103203381..103208955hg38UCSC Ensembl
Innerchr9:105965663..105971237hg19UCSC Ensembl
Innerchr9:105005484..105011058hg18UCSC Ensembl
Innerchr9:103045218..103050792hg17UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg385575
hg195575
hg185575
hg175575
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516844
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695601
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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