A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6347892



Internal ID21005445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:7807468..7810153hg38UCSC Ensembl
chr2:7947599..7950284hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg382686
hg192686
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18090715
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6347892
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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