A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17987790



Internal ID20554830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:12417728..12421928hg38UCSC Ensembl
chr11:12439275..12443475hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg384201
hg194201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6446518
Supporting Variants
Samples
Known GenesPARVA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17987790
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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