A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007665



Internal ID19096884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:21740235..21767774hg38UCSC Ensembl
Innerchr3:21781727..21809266hg19UCSC Ensembl
Innerchr3:21756731..21784270hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3827540
hg1927540
hg1827540
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3593153
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)nsv1007665
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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