A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6863



Internal ID15205129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:37318664..37351668hg38UCSC Ensembl
OuterchrX:37177917..37210921hg19UCSC Ensembl
OuterchrX:37062838..37095842hg18UCSC Ensembl
OuterchrX:36934111..36967115hg17UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg386434
hg196434
hg186434
hg176434
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6321
SamplesNA12156
Known GenesPRRG1
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)nsv6863
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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