A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1155846



Internal ID15853735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:39979094..40093445hg38UCSC Ensembl
Innerchr7:40018693..40133044hg19UCSC Ensembl
Innerchr7:39985218..40099569hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38114352
hg19114352
hg18114352
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv606706
Supporting Variants
Samples1780854393_A
Known GenesCDK13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1155846
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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