A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6307



Internal ID15537556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:9402078..9416896hg38UCSC Ensembl
OuterchrX:9370118..9384936hg19UCSC Ensembl
OuterchrX:9330118..9344936hg18UCSC Ensembl
OuterchrX:9179854..9194672hg17UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg3813982
hg1913982
hg1813982
hg1713982
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6792
Supporting Variants
SamplesNA12156
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)nssv6307
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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