A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3689104



Internal ID18987385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:7192313..7288729hg38UCSC Ensembl
Innerchr9:7192313..7288729hg19UCSC Ensembl
Innerchr9:7182313..7278729hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3896417
hg1996417
hg1896417
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1021049
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)nssv3689104
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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