A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6382



Internal ID15190796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:139978995..140216348hg38UCSC Ensembl
OuterchrX:139061154..139298500hg19UCSC Ensembl
OuterchrX:138888820..139126166hg18UCSC Ensembl
OuterchrX:138786674..139024020hg17UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg38237354
hg19237347
hg18237347
hg17237347
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7461
Supporting Variants
SamplesNA12156
Known GenesLOC389895
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)nssv6382
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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