A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601898



Internal ID20974969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:99725101..99836200hg38UCSC Ensembl
chr6:100172977..100284076hg19UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg38111100
hg19111100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18147653
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601898
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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