A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029738



Internal ID18772269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:185450051..185515559hg38UCSC Ensembl
Innerchr4:186371205..186436713hg19UCSC Ensembl
Innerchr4:186608199..186673707hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3865509
hg1965509
hg1865509
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635617
Samples
Known GenesCCDC110, PDLIM3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029738
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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