A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369037



Internal ID21026590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:6627605..6628702hg38UCSC Ensembl
chr4:6629332..6630429hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg381098
hg191098
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18119352
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369037
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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