A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6355547



Internal ID21013100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:66448001..66450100hg38UCSC Ensembl
chr2:66675133..66677232hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18090064
Samples
Known GenesMEIS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6355547
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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