A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3959780



Internal ID18878815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:52756023..52761123hg38UCSC Ensembl
OuterchrX:52785100..52790200hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg385101
hg195101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1119340
Supporting Variants
SamplesKWS1
Known GenesSSX2, SSX2B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3959780
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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