A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17422509



Internal ID22480379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:95840206..95846207hg38UCSC Ensembl
chr4:96761357..96767358hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg386002
hg196002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5891101
Supporting Variants
Samples
Known GenesPDHA2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17422509
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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