A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057596



Internal ID19146815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:24201148..24338821hg38UCSC Ensembl
Innerchr19:24383950..24521623hg19UCSC Ensembl
Innerchr19:24175790..24313463hg18UCSC Ensembl
Cytoband19p11
Allele length
AssemblyAllele length
hg38137674
hg19137674
hg18137674
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3485n100
Supporting Variantsnssv3570688
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)nsv1057596
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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