A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3498439



Internal ID19086080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:190028927..190087425hg38UCSC Ensembl
Innerchr1:189998057..190056555hg19UCSC Ensembl
Innerchr1:188264680..188323178hg18UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg3858499
hg1958499
hg1858499
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1012448
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)nssv3498439
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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