A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3625142



Internal ID18923423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:49050193..49295206hg38UCSC Ensembl
Innerchr4:49052210..49297223hg19UCSC Ensembl
Innerchr4:48746967..48991980hg18UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg38245014
hg19245014
hg18245014
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1012915
Supporting Variants
Samples
Known GenesCWH43
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3625142
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer