A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6395809



Internal ID21053362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:8676984..8725253hg38UCSC Ensembl
chr6:8677217..8725486hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg3848270
hg1948270
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18149050
Samples
Known GenesLOC100506207
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6395809
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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