A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6108743



Internal ID22017977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:136247726..136253949hg38UCSC Ensembl
chrX:135329885..135336108hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg386224
hg196224
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17646714
Samples
Known GenesMAP7D3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6108743
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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