A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3930613



Internal ID21350682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:101900284..101900336hg38UCSC Ensembl
chrX:101155257..101155309hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15199912
SamplesHG002
Known GenesZMAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3930613
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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