A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3639341



Internal ID18937622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:118204206..118650082hg38UCSC Ensembl
Innerchr4:119125361..119571237hg19UCSC Ensembl
Innerchr4:119344809..119790685hg18UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38445877
hg19445877
hg18445877
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1002771
Supporting Variants
Samples
Known GenesCEP170P1, LOC729218, NDST3, PRSS12, SNHG8, SNORA24
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3639341
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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