A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv882



Internal ID15198402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:68640299..68674421hg38UCSC Ensembl
OuterchrX:67860141..67894263hg19UCSC Ensembl
OuterchrX:67776866..67810988hg18UCSC Ensembl
OuterchrX:67643162..67677284hg17UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg386874
hg196874
hg186874
hg176874
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6943
Supporting Variants
SamplesNA19240
Known GenesSTARD8
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)nssv882
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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