A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6354214



Internal ID21011767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:136011759..136013183hg38UCSC Ensembl
chr2:136769329..136770753hg19UCSC Ensembl
Cytoband2q21.3
Allele length
AssemblyAllele length
hg381425
hg191425
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18077914
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6354214
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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