A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001287



Internal ID19090504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:25532518..25572239hg38UCSC Ensembl
Innerchr4:25534140..25573861hg19UCSC Ensembl
Innerchr4:25143238..25182959hg18UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3839722
hg1939722
hg1839722
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5158n100
Supporting Variantsnssv3620599
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)nsv1001287
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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