A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7114



Internal ID15552091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:138523278..138554926hg38UCSC Ensembl
OuterchrX:137605439..137637087hg19UCSC Ensembl
OuterchrX:137433105..137464753hg18UCSC Ensembl
OuterchrX:137330959..137362607hg17UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg3831649
hg1931649
hg1831649
hg1731649
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8790
SamplesNA12156
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)nsv7114
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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