A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9782



Internal ID15193152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:120872639..120987694hg38UCSC Ensembl
OuterchrX:120006493..120121548hg19UCSC Ensembl
OuterchrX:119890521..119949229hg18UCSC Ensembl
OuterchrX:119788375..119847083hg17UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38115056
hg19115056
hg1858709
hg1758709
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7061
Supporting Variants
SamplesNA18507
Known GenesCT47A1, CT47A10, CT47A11, CT47A12, CT47A2, CT47A3, CT47A4, CT47A5, CT47A6, CT47A7, CT47A8, CT47A9, CT47B1
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)nssv9782
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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