A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032153



Internal ID19121375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:74880301..74915335hg38UCSC Ensembl
Innerchr6:75590017..75625051hg19UCSC Ensembl
Innerchr6:75646737..75681771hg18UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3835035
hg1935035
hg1835035
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3658818
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)nsv1032153
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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