A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604257



Internal ID16391666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:99586756..99587280hg38UCSC Ensembl
Innerchr6:100034632..100035156hg19UCSC Ensembl
Innerchr6:100141353..100141877hg18UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg38525
hg19525
hg18525
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10861n54
Supporting Variantsnssv1070553, nssv1070550, nssv1070552, nssv1070551
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604257
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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