A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6952



Internal ID15205227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:71043021..71077533hg38UCSC Ensembl
OuterchrX:70262871..70297383hg19UCSC Ensembl
OuterchrX:70179596..70214108hg18UCSC Ensembl
OuterchrX:70045892..70080404hg17UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg386485
hg196485
hg186485
hg176485
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv883
SamplesNA19240
Known GenesSNX12
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)nsv6952
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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