A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609021



Internal ID20982092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:137435348..137435576hg38UCSC Ensembl
chr6:137756485..137756713hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38229
hg19229
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18138335
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609021
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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