A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6340281



Internal ID20997834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:67502101..67505100hg38UCSC Ensembl
chr2:67729233..67732232hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18090167
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6340281
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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