A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6332



Internal ID15537531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:53331714..53366112hg38UCSC Ensembl
OuterchrX:53360919..53393032hg19UCSC Ensembl
OuterchrX:53377644..53409757hg18UCSC Ensembl
OuterchrX:53243940..53276053hg17UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg387326
hg197326
hg187326
hg177326
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6907
Supporting Variants
SamplesNA12156
Known GenesMIR5684
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)nssv6332
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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