A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6398678



Internal ID21056231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:76300492..76307364hg38UCSC Ensembl
chr6:77010209..77017081hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg386873
hg196873
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18148172
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6398678
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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