A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001118



Internal ID19090335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:34759898..34844007hg38UCSC Ensembl
Innerchr4:34761520..34845629hg19UCSC Ensembl
Innerchr4:34437915..34522024hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3884110
hg1984110
hg1884110
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5165n100
Supporting Variantsnssv3620675
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)nsv1001118
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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