A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3987538



Internal ID19205357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:1518007..1532907hg38UCSC Ensembl
OuterchrX:1636900..1651800hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3814901
hg1914901
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1132748
Supporting Variants
SamplesKWS1
Known GenesP2RY8
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3987538
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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