A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6341



Internal ID15190837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:72739843..72942208hg38UCSC Ensembl
OuterchrX:71959667..72162047hg19UCSC Ensembl
OuterchrX:71876392..72078772hg18UCSC Ensembl
OuterchrX:71742688..71945068hg17UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg38202366
hg19202381
hg18202381
hg17202381
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7450
Supporting Variants
SamplesNA12156
Known GenesDMRTC1, DMRTC1B, FAM226A, FAM226B, LINC00684
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)nssv6341
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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