A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10775



Internal ID15195337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:97883383..97915393hg38UCSC Ensembl
Outerchr10:99643140..99675150hg19UCSC Ensembl
Outerchr10:99633130..99665140hg18UCSC Ensembl
Outerchr10:99633130..99665140hg17UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg387487
hg197487
hg187487
hg177487
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7510
Supporting Variants
SamplesNA18956
Known GenesCRTAC1
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)nssv10775
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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