A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3615255



Internal ID18913536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:29013..121227hg38UCSC Ensembl
Innerchr4:29013..121107hg19UCSC Ensembl
Innerchr4:19013..111107hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3892215
hg1992095
hg1892095
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1004788
Supporting Variants
Samples
Known GenesZNF595, ZNF718
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3615255
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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