A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517747



Internal ID15445040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:56536464..56713975hg38UCSC Ensembl
Innerchr10:58296224..58473735hg19UCSC Ensembl
Innerchr10:57966230..58143741hg18UCSC Ensembl
Innerchr10:57966230..58143741hg17UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38177512
hg19177512
hg18177512
hg17177512
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv679017, nssv653089, nssv655682, nssv691841, nssv688516, nssv687651, nssv671113, nssv662097, nssv657393, nssv682903
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517747
Frequency
Sample Size2026
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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