A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3625037



Internal ID18576632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:39916983..40113619hg38UCSC Ensembl
Innerchr4:39918603..40115239hg19UCSC Ensembl
Innerchr4:39594998..39791634hg18UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38196637
hg19196637
hg18196637
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1014191
Supporting Variants
Samples
Known GenesLOC344967, N4BP2, PDS5A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3625037
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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