A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17495625



Internal ID22553558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:141332696..141341054hg38UCSC Ensembl
chr5:140712263..140720621hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg388359
hg198359
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5841704
Supporting Variants
Samples
Known GenesPCDHGA1, PCDHGA2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17495625
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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