A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5425697



Internal ID204654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:69891178..69891545hg38UCSC Ensembl
chrX:69111009..69111376hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg38368
hg19368
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17740586
Samples
Known GenesEDA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5425697
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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