A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6111268



Internal ID22020501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:20094505..20094569hg38UCSC Ensembl
chrX:20112623..20112687hg19UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17646585
Samples
Known GenesMAP7D2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6111268
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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