A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6342



Internal ID15190836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:72800310..72879544hg38UCSC Ensembl
OuterchrX:72020144..72099379hg19UCSC Ensembl
OuterchrX:71936869..72016104hg18UCSC Ensembl
OuterchrX:71803165..71882400hg17UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3879235
hg1979236
hg1879236
hg1779236
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7450
Supporting Variants
SamplesNA12156
Known GenesDMRTC1, DMRTC1B
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)nssv6342
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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