A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8840



Internal ID15535024
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 StatusS
Merged Variantsnsv7533
Supporting Variants
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)nssv8840
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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