A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6614685



Internal ID20987756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:99260578..99264754hg38UCSC Ensembl
chr6:99708454..99712630hg19UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg384177
hg194177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18147624
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6614685
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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