A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3697594



Internal ID18995875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:102807930..102992459hg38UCSC Ensembl
Innerchr9:105570212..105754741hg19UCSC Ensembl
Innerchr9:104610033..104794562hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38184530
hg19184530
hg18184530
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1054263
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)nssv3697594
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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