A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18144029



Internal ID20711069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:52863100..52870819hg38UCSC Ensembl
chr6:52727898..52735617hg19UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg387720
hg197720
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6411436
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18144029
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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