A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5423951



Internal ID202957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:130207326..130207398hg38UCSC Ensembl
chrX:129341300..129341372hg19UCSC Ensembl
CytobandXq26.1
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17737566
Samples
Known GenesZNF280C
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5423951
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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