A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6377



Internal ID15190801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:135148445..135261952hg38UCSC Ensembl
OuterchrX:134282372..134395899hg19UCSC Ensembl
OuterchrX:134110038..134223565hg18UCSC Ensembl
OuterchrX:134007892..134121419hg17UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38113508
hg19113528
hg18113528
hg17113528
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)nssv6377
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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