A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8684



Internal ID15535180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:9581613..9626255hg38UCSC Ensembl
OuterchrX:9549653..9594295hg19UCSC Ensembl
OuterchrX:9509653..9554295hg18UCSC Ensembl
OuterchrX:9359389..9404031hg17UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3844643
hg1944643
hg1844643
hg1744643
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6793
Supporting Variants
SamplesNA12156
Known GenesTBL1X
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)nssv8684
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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