A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3487893



Internal ID19075534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:194174185..194412005hg38UCSC Ensembl
Innerchr1:194143315..194381135hg19UCSC Ensembl
Innerchr1:192409938..192647758hg18UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg38237821
hg19237821
hg18237821
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1004338
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)nssv3487893
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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