A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5426709



Internal ID205633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:7067596..7196706hg38UCSC Ensembl
chrX:6985637..7114747hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38129111
hg19129111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17739099
Samples
Known GenesHDHD1, MIR4767
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5426709
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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