A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7088



Internal ID15205376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:71422827..71455204hg38UCSC Ensembl
Outerchr10:73182584..73214961hg19UCSC Ensembl
Outerchr10:72852590..72884967hg18UCSC Ensembl
Outerchr10:72852590..72884967hg17UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg386879
hg196879
hg186879
hg176879
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5296
SamplesNA19129
Known GenesCDH23
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)nsv7088
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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