A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6400347



Internal ID21057900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:4576613..4589150hg38UCSC Ensembl
chr6:4576847..4589384hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg3812538
hg1912538
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18144193
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6400347
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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