A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001610



Internal ID19090827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:24337..63403hg38UCSC Ensembl
Innerchr3:66011..105086hg19UCSC Ensembl
Innerchr3:41011..80086hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3839067
hg1939076
hg1839076
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4601n100
Supporting Variantsnssv3590220
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)nsv1001610
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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