A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3697580



Internal ID18995861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:102144997..102217289hg38UCSC Ensembl
Innerchr9:104907279..104979571hg19UCSC Ensembl
Innerchr9:103947100..104019392hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3872293
hg1972293
hg1872293
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1051091
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)nssv3697580
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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