A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3961783



Internal ID19206393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:156020235..156023035hg38UCSC Ensembl
OuterchrX:155249900..155252700hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg382801
hg192801
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1129109
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3961783
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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