A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997455



Internal ID19156991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:51819521..51838330hg38UCSC Ensembl
Innerchr4:52685687..52704496hg19UCSC Ensembl
Innerchr4:52380444..52399253hg18UCSC Ensembl
Cytoband4q11
Allele length
AssemblyAllele length
hg3818810
hg1918810
hg1818810
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3625257, nssv3625256
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)nsv997455
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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