A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602368



Internal ID16389777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32506157..32516591hg38UCSC Ensembl
Innerchr6:32473934..32484368hg19UCSC Ensembl
Innerchr6:32581912..32592346hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3810435
hg1910435
hg1810435
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10520n54
Supporting Variantsnssv1055256, nssv1055274, nssv1055263, nssv1055251, nssv1055264, nssv1055255, nssv1055250, nssv1055248, nssv1055258, nssv1055259, nssv1055249, nssv1055266, nssv1055269, nssv1055268, nssv1055271, nssv1055246, nssv1055273, nssv1055257, nssv1055270, nssv1055253, nssv1055254, nssv1055262, nssv1055247, nssv1055261, nssv1055260, nssv1055267, nssv1055272, nssv1055265, nssv1055252
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602368
Frequency
Sample Size17421
Observed Gain0
Observed Loss29
Observed Complex0
Frequencyn/a


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