A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3961752



Internal ID19206151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:51259837..51268237hg38UCSC Ensembl
OuterchrX:51002700..51011100hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg388401
hg198401
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1129079
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3961752
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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