A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17739524



Internal ID163190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:19107000..19117600hg38UCSC Ensembl
chrX:19125118..19135718hg19UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg3810601
hg1910601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138477
Supporting Variants
Samples
Known GenesGPR64
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17739524
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00209161


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