A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602421



Internal ID16389830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32526201..32530183hg38UCSC Ensembl
Innerchr6:32493978..32497960hg19UCSC Ensembl
Innerchr6:32601956..32605938hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg383983
hg193983
hg183983
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10532n54
Supporting Variantsnssv1055537, nssv1055541, nssv1055555, nssv1055545, nssv1055530, nssv1055533, nssv1055534, nssv1055544, nssv1055548, nssv1055527, nssv1055542, nssv1055535, nssv1055553, nssv1055536, nssv1055529, nssv1055549, nssv1055559, nssv1055538, nssv1055560, nssv1055551, nssv1055532, nssv1055550, nssv1055558, nssv1055554, nssv1055528, nssv1055546, nssv1055543, nssv1055539, nssv1055540, nssv1055556, nssv1055526, nssv1055531, nssv1055557, nssv1055547, nssv1055552
Samples
Known GenesHLA-DRB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602421
Frequency
Sample Size17421
Observed Gain0
Observed Loss35
Observed Complex0
Frequencyn/a


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