A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3977880



Internal ID19236355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:1641307..1642607hg38UCSC Ensembl
OuterchrX:1760200..1761500hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg381301
hg191301
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1125074
Supporting Variants
SamplesKWS2
Known GenesASMT
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3977880
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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