A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7528



Internal ID15205860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:103062273..103106919hg38UCSC Ensembl
Outerchr10:104822030..104866676hg19UCSC Ensembl
Outerchr10:104812020..104856666hg18UCSC Ensembl
Outerchr10:104812020..104856666hg17UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg3844647
hg1944647
hg1844647
hg1744647
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1907
SamplesNA18555
Known GenesCNNM2, NT5C2
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nsv7528
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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