A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517606



Internal ID15444899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:149423496..149434559hg38UCSC Ensembl
Innerchr6:149744632..149755695hg19UCSC Ensembl
Innerchr6:149786325..149797388hg18UCSC Ensembl
Innerchr6:149786325..149797388hg17UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3811064
hg1911064
hg1811064
hg1711064
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv680058, nssv658235, nssv691855, nssv657428, nssv662331, nssv670052, nssv665597, nssv652492, nssv674035, nssv668859, nssv669981, nssv657999, nssv675972, nssv671555
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517606
Frequency
Sample Size2026
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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