A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6337067



Internal ID20994620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:11558947..11564589hg38UCSC Ensembl
chr2:11699073..11704715hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg385643
hg195643
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18075738
Samples
Known GenesGREB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6337067
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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