A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18096439



Internal ID20663479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155657925..155664688hg38UCSC Ensembl
chr3:155375714..155382477hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg386764
hg196764
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6358675
Supporting Variants
Samples
Known GenesPLCH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18096439
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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