A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6354565



Internal ID21012118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:85006598..85023572hg38UCSC Ensembl
chr2:85233721..85250695hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg3816975
hg1916975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18091118
Samples
Known GenesKCMF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6354565
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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