A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604826



Internal ID16045549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:145383210..145385252hg38UCSC Ensembl
Innerchr6:145704346..145706388hg19UCSC Ensembl
Innerchr6:145746039..145748081hg18UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg382043
hg192043
hg182043
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10961n54
Supporting Variantsnssv1074256, nssv1074258, nssv1074257
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604826
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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