A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6795



Internal ID15551740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:10230791..10262987hg38UCSC Ensembl
OuterchrX:10198831..10231027hg19UCSC Ensembl
OuterchrX:10158831..10191027hg18UCSC Ensembl
OuterchrX:10008567..10040763hg17UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg387086
hg197086
hg187086
hg177086
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5200
SamplesNA19129
Known GenesCLCN4
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)nsv6795
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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