A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001578



Internal ID18744109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:12269..68917hg38UCSC Ensembl
Innerchr4:12269..68809hg19UCSC Ensembl
Innerchr4:2269..58809hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3856649
hg1956541
hg1856541
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5056n100
Supporting Variantsnssv3615144
Samples
Known GenesZNF595, ZNF718
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1001578
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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