A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1832



Internal ID15541115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:44657239..44685897hg38UCSC Ensembl
OuterchrX:44516485..44545143hg19UCSC Ensembl
OuterchrX:44401429..44430087hg18UCSC Ensembl
OuterchrX:44272739..44301397hg17UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg3828659
hg1928659
hg1828659
hg1728659
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6881
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)nssv1832
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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