A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8690



Internal ID15188488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:14836320..14868456hg38UCSC Ensembl
OuterchrX:14854442..14886578hg19UCSC Ensembl
OuterchrX:14764363..14796499hg18UCSC Ensembl
OuterchrX:14614099..14646235hg17UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3832137
hg1932137
hg1832137
hg1732137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6812
Supporting Variants
SamplesNA12156
Known GenesFANCB
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)nssv8690
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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