A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007895



Internal ID19097114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:13171316..13217385hg38UCSC Ensembl
Innerchr3:13212816..13258885hg19UCSC Ensembl
Innerchr3:13187816..13233885hg18UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3846070
hg1946070
hg1846070
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3593082
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)nsv1007895
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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