A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10714



Internal ID15542084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:55688281..55704923hg38UCSC Ensembl
OuterchrX:55714714..55731356hg19UCSC Ensembl
OuterchrX:55731439..55748081hg18UCSC Ensembl
OuterchrX:55597735..55614377hg17UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg3816643
hg1916643
hg1816643
hg1716643
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6914
Supporting Variants
SamplesNA18956
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)nssv10714
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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