A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8713



Internal ID15535151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:41203238..41237093hg38UCSC Ensembl
OuterchrX:41062491..41096346hg19UCSC Ensembl
OuterchrX:40947435..40981290hg18UCSC Ensembl
OuterchrX:40818745..40852600hg17UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg385572
hg195572
hg185572
hg175572
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6874
Supporting Variants
SamplesNA12156
Known GenesUSP9X
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)nssv8713
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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