A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3635656



Internal ID18587251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:187514678..188135966hg38UCSC Ensembl
Innerchr4:188435832..189057120hg19UCSC Ensembl
Innerchr4:188672826..189294114hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38621289
hg19621289
hg18621289
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1025366
Supporting Variants
Samples
Known GenesTRIML2, ZFP42
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3635656
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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