A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012736



Internal ID19101953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:21934529..21959454hg38UCSC Ensembl
Innerchr3:21976021..22000946hg19UCSC Ensembl
Innerchr3:21951025..21975950hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3824926
hg1924926
hg1824926
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4695n100
Supporting Variantsnssv3593163
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)nsv1012736
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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