A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601241



Internal ID16041964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29865764..29901207hg38UCSC Ensembl
Innerchr6:29833541..29868984hg19UCSC Ensembl
Innerchr6:29941520..29976963hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3835444
hg1935444
hg1835444
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1154039, nssv1154040, nssv1051732, nssv1051733
SamplesHGDP00098, HGDP00058
Known GenesHLA-H
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601241
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer