A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7527



Internal ID15205859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:102805716..102839530hg38UCSC Ensembl
Outerchr10:104565473..104599287hg19UCSC Ensembl
Outerchr10:104555463..104589277hg18UCSC Ensembl
Outerchr10:104555463..104589277hg17UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg385620
hg195620
hg185620
hg175620
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8838
SamplesNA12156
Known GenesCYP17A1, WBP1L
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)nsv7527
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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