A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6336565



Internal ID20994118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:88861556..89234188hg38UCSC Ensembl
chr2:89161068..89533669hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38372633
hg19372602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3977n223
Supporting Variantsnssv18091844
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6336565
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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