A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602156



Internal ID16389565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32487705..32513730hg38UCSC Ensembl
Innerchr6:32455482..32481507hg19UCSC Ensembl
Innerchr6:32563460..32589485hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3826026
hg1926026
hg1826026
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10500n54
Supporting Variantsnssv1053974, nssv1053973, nssv1053982, nssv1053985, nssv1053970, nssv1053978, nssv1053971, nssv1053975, nssv1053969, nssv1053981, nssv1053980, nssv1053977, nssv1053979, nssv1053972, nssv1053976, nssv1053988, nssv1053984, nssv1053986, nssv1053987, nssv1053983
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602156
Frequency
Sample Size17421
Observed Gain0
Observed Loss20
Observed Complex0
Frequencyn/a


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