A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3961755



Internal ID19220101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:62462730..62470930hg38UCSC Ensembl
OuterchrX:61682200..61690400hg19UCSC Ensembl
CytobandXq11.1
Allele length
AssemblyAllele length
hg388201
hg198201
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1129082
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3961755
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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