A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517656



Internal ID15444949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:125203747..125218374hg38UCSC Ensembl
Innerchr11:125073643..125088270hg19UCSC Ensembl
Innerchr11:124578853..124593480hg18UCSC Ensembl
Innerchr11:124578853..124593480hg17UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3814628
hg1914628
hg1814628
hg1714628
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv83n21
Supporting Variantsnssv692665, nssv668344, nssv657436, nssv682105, nssv687764, nssv674710, nssv661922, nssv662618, nssv660769, nssv660239, nssv654823, nssv688479, nssv655022, nssv652796, nssv669334, nssv677747, nssv690174, nssv671513, nssv664469, nssv652683, nssv683735, nssv655662, nssv655441, nssv704669, nssv657525, nssv669420, nssv671167, nssv657760, nssv659047
Samples
Known GenesPKNOX2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517656
Frequency
Sample Size2026
Observed Gain0
Observed Loss29
Observed Complex0
Frequencyn/a


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