A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6790



Internal ID15551735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:8931696..8965630hg38UCSC Ensembl
OuterchrX:8899737..8933671hg19UCSC Ensembl
OuterchrX:8859737..8893671hg18UCSC Ensembl
OuterchrX:8709473..8743407hg17UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg385802
hg195802
hg185802
hg175802
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3764
SamplesNA12878
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)nsv6790
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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