A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6889



Internal ID15551843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:47723800..47757687hg38UCSC Ensembl
OuterchrX:47583199..47617086hg19UCSC Ensembl
OuterchrX:47468143..47502030hg18UCSC Ensembl
OuterchrX:47339453..47373340hg17UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3827239
hg1927239
hg1827239
hg1727239
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2831, nssv9481
SamplesNA18555, NA18517
Known GenesCXXC1P1
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)nsv6889
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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