A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035620



Internal ID18778151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73984364..74050155hg38UCSC Ensembl
Innerchr14:74451067..74516858hg19UCSC Ensembl
Innerchr14:73520820..73586611hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3865792
hg1965792
hg1865792
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1938n100
Supporting Variantsnssv3531164
Samples
Known GenesCCDC176, ENTPD5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035620
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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