A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3765938



Internal ID19305586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:101541612..101545613hg38UCSC Ensembl
chrX:100796599..100800600hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg384002
hg194002
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1078123
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3765938
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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