A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6101064



Internal ID22010297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:70208850..70234170hg38UCSC Ensembl
chrX:69428700..69454020hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3825321
hg1925321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17641071
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6101064
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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