A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6354885



Internal ID21012438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:180575701..180576800hg38UCSC Ensembl
chr2:181440428..181441527hg19UCSC Ensembl
Cytoband2q31.3
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18081090
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6354885
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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