A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3525612



Internal ID18823893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:112350824..112380487hg38UCSC Ensembl
Innerchr13:113005138..113034801hg19UCSC Ensembl
Innerchr13:112053139..112082802hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3829664
hg1929664
hg1829664
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050682
Supporting Variants
Samples
Known GenesSPACA7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3525612
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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