A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6354862



Internal ID21012415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:66560765..66561534hg38UCSC Ensembl
chr2:66787897..66788666hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg38770
hg19770
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18090071
Samples
Known GenesMEIS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6354862
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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