A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3937470



Internal ID21357540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:84191839..84198031hg38UCSC Ensembl
chrX:83446847..83453039hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg386193
hg196193
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15200228
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3937470
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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