A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6381



Internal ID15537482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:137038705..137084291hg38UCSC Ensembl
OuterchrX:136120864..136166450hg19UCSC Ensembl
OuterchrX:135948530..135994116hg18UCSC Ensembl
OuterchrX:135846384..135891970hg17UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg3845587
hg1945587
hg1845587
hg1745587
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7111
Supporting Variants
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)nssv6381
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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