A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3986993



Internal ID19215911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:47090914..47090966hg38UCSC Ensembl
OuterchrX:46950313..46950365hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1132239
Supporting Variants
SamplesKWS1
Known GenesRGN
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3986993
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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