A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010460



Internal ID19099677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:21475318..21798379hg38UCSC Ensembl
Innerchr3:21516810..21839871hg19UCSC Ensembl
Innerchr3:21491814..21814875hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38323062
hg19323062
hg18323062
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3593149
Samples
Known GenesZNF385D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010460
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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