A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17446320



Internal ID22504190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:15412486..15412687hg38UCSC Ensembl
chrX:15430608..15430809hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38202
hg19202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5885801
Supporting Variants
Samples
Known GenesPIR, PIR-FIGF
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17446320
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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