A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611446



Internal ID16398855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:62303056..62310322hg38UCSC Ensembl
Innerchr8:63215615..63222881hg19UCSC Ensembl
Innerchr8:63378169..63385435hg18UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg387267
hg197267
hg187267
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156847, nssv1156848, nssv1156849
SamplesHGDP00993, HGDP01286, HGDP00915
Known GenesNKAIN3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611446
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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