A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18136161



Internal ID20703201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:93620201..93621900hg38UCSC Ensembl
chr5:92955907..92957606hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6398063
Supporting Variants
Samples
Known GenesFAM172A, MIR2277, MIR548AO
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18136161
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00063


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