A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517486



Internal ID15444779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:6612823..6803275hg38UCSC Ensembl
Innerchr10:6654785..6845237hg19UCSC Ensembl
Innerchr10:6694791..6885243hg18UCSC Ensembl
Innerchr10:6694791..6885243hg17UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38190453
hg19190453
hg18190453
hg17190453
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv689867, nssv682481, nssv685112, nssv679163, nssv691967, nssv701295, nssv674140, nssv652162, nssv677978, nssv674359, nssv674968, nssv689480, nssv684180, nssv682252
Samples
Known GenesLINC00706, LINC00707
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517486
Frequency
Sample Size2026
Observed Gain4
Observed Loss10
Observed Complex0
Frequencyn/a


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