A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv849



Internal ID15544847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:9405216..9406242hg38UCSC Ensembl
OuterchrX:9373256..9374282hg19UCSC Ensembl
OuterchrX:9333256..9334282hg18UCSC Ensembl
OuterchrX:9182992..9184018hg17UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg3827422
hg1927422
hg1827422
hg1727422
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6792
Supporting Variants
SamplesNA19240
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)nssv849
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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