A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601938



Internal ID20975009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166375391..166385602hg38UCSC Ensembl
chr6:166788879..166799090hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3810212
hg1910212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143040
Samples
Known GenesMPC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601938
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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