A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3927185



Internal ID21347254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:84874715..84874914hg38UCSC Ensembl
chrX:84129721..84129920hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg38200
hg19200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15200229
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3927185
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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