A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604237



Internal ID16391646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:95433859..95500984hg38UCSC Ensembl
Innerchr6:95881735..95948860hg19UCSC Ensembl
Innerchr6:95988456..96055581hg18UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3867126
hg1967126
hg1867126
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1069239
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604237
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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