A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8801



Internal ID15535063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:69603455..69637500hg38UCSC Ensembl
Outerchr10:71363211..71397256hg19UCSC Ensembl
Outerchr10:71033217..71067262hg18UCSC Ensembl
Outerchr10:71033217..71067262hg17UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg385393
hg195393
hg185393
hg175393
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7032
Supporting Variants
SamplesNA12156
Known GenesC10orf35
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)nssv8801
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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