A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6877



Internal ID15551830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:42948174..42982722hg38UCSC Ensembl
OuterchrX:42807423..42841971hg19UCSC Ensembl
OuterchrX:42692367..42726915hg18UCSC Ensembl
OuterchrX:42563677..42598225hg17UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg385476
hg195476
hg185476
hg175476
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2829
SamplesNA18555
Known Genes
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)nsv6877
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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