A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6801



Internal ID15551747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:12049442..12083561hg38UCSC Ensembl
OuterchrX:12067561..12101680hg19UCSC Ensembl
OuterchrX:11977482..12011601hg18UCSC Ensembl
OuterchrX:11827218..11861337hg17UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg385905
hg195905
hg185905
hg175905
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2827
SamplesNA18555
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)nsv6801
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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