A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5420452



Internal ID199557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:152938650..152938912hg38UCSC Ensembl
chrX:152107194..152107456hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38263
hg19263
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738043
Samples
Known GenesZNF185
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5420452
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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