A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3986994



Internal ID18858191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:47233763..47233816hg38UCSC Ensembl
OuterchrX:47093162..47093215hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1139400
Supporting Variants
SamplesKWS1
Known GenesUSP11
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3986994
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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