A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6338127



Internal ID20995680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:6638431..6644651hg38UCSC Ensembl
chr2:6778563..6784783hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg386221
hg196221
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18090059
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6338127
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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