A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3987545



Internal ID19210794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:25308183..25319183hg38UCSC Ensembl
OuterchrX:25326300..25337300hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg3811001
hg1911001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1132755
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3987545
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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