A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6376



Internal ID15190802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:135147190..135186536hg38UCSC Ensembl
OuterchrX:134281117..134320464hg19UCSC Ensembl
OuterchrX:134108783..134148130hg18UCSC Ensembl
OuterchrX:134006637..134045984hg17UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg3839347
hg1939348
hg1839348
hg1739348
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7458
Supporting Variants
SamplesNA12156
Known GenesCXorf48
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)nssv6376
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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