A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3625145



Internal ID18923426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:49078984..49307825hg38UCSC Ensembl
Innerchr4:49081001..49309842hg19UCSC Ensembl
Innerchr4:48775758..49004599hg18UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg38228842
hg19228842
hg18228842
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1002272
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3625145
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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