A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv879



Internal ID15545072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:64053623..64088654hg38UCSC Ensembl
OuterchrX:63273503..63308534hg19UCSC Ensembl
OuterchrX:63190228..63225259hg18UCSC Ensembl
OuterchrX:63056524..63091555hg17UCSC Ensembl
CytobandXq11.1
Allele length
AssemblyAllele length
hg385967
hg195967
hg185967
hg175967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6928
Supporting Variants
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)nssv879
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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