A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5419764



Internal ID198888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:7249670..7250883hg38UCSC Ensembl
chrX:7167711..7168924hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg381214
hg191214
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17739105
Samples
Known GenesSTS
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5419764
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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