A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3689111



Internal ID18987392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:7731398..7773114hg38UCSC Ensembl
Innerchr9:7731398..7773114hg19UCSC Ensembl
Innerchr9:7721398..7763114hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3841717
hg1941717
hg1841717
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1034997
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3689111
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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