A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7533



Internal ID15205866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:104229889..104253571hg38UCSC Ensembl
Outerchr10:105989647..106013329hg19UCSC Ensembl
Outerchr10:105979637..106003319hg18UCSC Ensembl
Outerchr10:105979637..106003319hg17UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg386069
hg196069
hg186069
hg176069
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8840
SamplesNA12156
Known GenesWDR96
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)nsv7533
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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