A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517617



Internal ID15444910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:78383140..78417941hg38UCSC Ensembl
Innerchr18:76143140..76177941hg19UCSC Ensembl
Innerchr18:74244128..74278929hg18UCSC Ensembl
Innerchr18:74244128..74278929hg17UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3834802
hg1934802
hg1834802
hg1734802
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv652554, nssv690817, nssv701361, nssv666283, nssv658169, nssv687973, nssv685066, nssv691651, nssv684545, nssv656729, nssv661017, nssv693633, nssv680999, nssv655503, nssv668700, nssv684525, nssv676297, nssv683519, nssv673506, nssv663830, nssv667994, nssv662425, nssv686712, nssv677300, nssv689790, nssv678345, nssv653365, nssv652532
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517617
Frequency
Sample Size2026
Observed Gain0
Observed Loss28
Observed Complex0
Frequencyn/a


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