A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517009



Internal ID15097616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:151983193..151987997hg38UCSC Ensembl
Innerchr6:152304328..152309132hg19UCSC Ensembl
Innerchr6:152346021..152350825hg18UCSC Ensembl
Innerchr6:152396442..152401246hg17UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg384805
hg194805
hg184805
hg174805
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv658461, nssv687271, nssv668063, nssv661083, nssv686535, nssv653605, nssv654972, nssv671067, nssv653217, nssv673802, nssv686848, nssv691880, nssv660390, nssv685311
Samples
Known GenesESR1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517009
Frequency
Sample Size2026
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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