A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997758



Internal ID19157295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:12269..45414hg38UCSC Ensembl
Innerchr4:12269..45410hg19UCSC Ensembl
Innerchr4:2269..35410hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3833146
hg1933142
hg1833142
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5051n100
Supporting Variantsnssv3619223, nssv3619204, nssv3619207, nssv3619205, nssv3619222, nssv3619208, nssv3619215, nssv3619219, nssv3619213, nssv3619212, nssv3619217, nssv3619216, nssv3619225, nssv3737918, nssv3619214, nssv3619209, nssv3619224, nssv3619210, nssv3619211, nssv3619206, nssv3619220, nssv3619203, nssv3619218, nssv3619221
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)nsv997758
Frequency
Sample Size11257
Observed Gain24
Observed Loss0
Observed Complex0
Frequencyn/a


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