A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6101635



Internal ID22010869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:72252666..72252748hg38UCSC Ensembl
chrX:71472516..71472598hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17644142
Samples
Known GenesPIN4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6101635
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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