A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3796



Internal ID15538523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:67892456..67915990hg38UCSC Ensembl
OuterchrX:67112298..67135832hg19UCSC Ensembl
OuterchrX:67029023..67052557hg18UCSC Ensembl
OuterchrX:66895319..66918853hg17UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg3823535
hg1923535
hg1823535
hg1723535
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6937
Supporting Variants
SamplesNA12878
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)nssv3796
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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