A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517549



Internal ID15098156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:73790158..73898823hg38UCSC Ensembl
Innerchr10:75549916..75658581hg19UCSC Ensembl
Innerchr10:75219922..75328587hg18UCSC Ensembl
Innerchr10:75219922..75328587hg17UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38108666
hg19108666
hg18108666
hg17108666
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv46n21
Supporting Variantsnssv678586, nssv658965, nssv660986, nssv678136, nssv701951, nssv698468, nssv652335, nssv679612
Samples
Known GenesCAMK2G, NDST2, ZSWIM8, ZSWIM8-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517549
Frequency
Sample Size2026
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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