A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517487



Internal ID15098094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86899290..86973435hg38UCSC Ensembl
Innerchr10:88659047..88733192hg19UCSC Ensembl
Innerchr10:88649027..88723172hg18UCSC Ensembl
Innerchr10:88649027..88723172hg17UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3874146
hg1974146
hg1874146
hg1774146
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv654899, nssv683797, nssv654749, nssv672583, nssv652165, nssv665892, nssv668658, nssv696694, nssv684561, nssv653325, nssv657453, nssv660010, nssv696782
Samples
Known GenesADIRF, AGAP11, BMPR1A, MMRN2, SNCG
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517487
Frequency
Sample Size2026
Observed Gain5
Observed Loss8
Observed Complex0
Frequencyn/a


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