A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6941



Internal ID15551901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:68597967..68631216hg38UCSC Ensembl
OuterchrX:67817809..67851058hg19UCSC Ensembl
OuterchrX:67734534..67767783hg18UCSC Ensembl
OuterchrX:67600830..67634079hg17UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg386757
hg196757
hg186757
hg176757
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1844
SamplesNA18555
Known Genes
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)nsv6941
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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