A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3959801



Internal ID19203805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:128776122..128788622hg38UCSC Ensembl
OuterchrX:127910100..127922600hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg3812501
hg1912501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1119361
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3959801
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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