A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3746681



Internal ID18698276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:177883324..178144253hg38UCSC Ensembl
Innerchr5:177310325..177571254hg19UCSC Ensembl
Innerchr5:177242931..177503860hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38260930
hg19260930
hg18260930
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1030383
Supporting Variants
Samples
Known GenesFAM153C, LOC728554, N4BP3, PROP1, RMND5B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3746681
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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