A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17440462



Internal ID22498332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:15808774..15808864hg38UCSC Ensembl
chrX:15826897..15826987hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5878191
Supporting Variants
Samples
Known GenesZRSR2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17440462
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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