A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6932



Internal ID15551891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:65881392..65913004hg38UCSC Ensembl
OuterchrX:65101234..65132846hg19UCSC Ensembl
OuterchrX:65017959..65049571hg18UCSC Ensembl
OuterchrX:64884255..64915867hg17UCSC Ensembl
CytobandXq11.2
Allele length
AssemblyAllele length
hg389385
hg199385
hg189385
hg179385
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv881
SamplesNA19240
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)nsv6932
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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