A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6866



Internal ID15205132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:38129794..38181944hg38UCSC Ensembl
OuterchrX:37989047..38041197hg19UCSC Ensembl
OuterchrX:37873991..37926141hg18UCSC Ensembl
OuterchrX:37745264..37797414hg17UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg3852151
hg1952151
hg1852151
hg1752151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8709, nssv1830
SamplesNA12156, NA18555
Known GenesSRPX
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)nsv6866
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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