A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3960245



Internal ID19212567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:2916559..2918359hg38UCSC Ensembl
OuterchrX:2834600..2836400hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg381801
hg191801
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1110591
Supporting Variants
SamplesKWS1
Known GenesARSD
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3960245
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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