A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6338725



Internal ID20996278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:66243101..66249700hg38UCSC Ensembl
chr2:66470233..66476832hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg386600
hg196600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3911n223
Supporting Variantsnssv18090049
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6338725
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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