A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6337672



Internal ID20995225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:61003081..61008936hg38UCSC Ensembl
chr2:61230216..61236071hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg385856
hg195856
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089451
Samples
Known GenesPUS10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6337672
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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