A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17460426



Internal ID22518310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:19080727..19083034hg38UCSC Ensembl
chrX:19098845..19101152hg19UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg382308
hg192308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5868580
Supporting Variants
Samples
Known GenesGPR64
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17460426
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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