A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1827



Internal ID15541110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:9405441..9406146hg38UCSC Ensembl
OuterchrX:9373481..9374186hg19UCSC Ensembl
OuterchrX:9333481..9334186hg18UCSC Ensembl
OuterchrX:9183217..9183922hg17UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg3830195
hg1930195
hg1830195
hg1730195
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6792
Supporting Variants
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)nssv1827
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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