A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6396330



Internal ID21053883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:6643045..6728792hg38UCSC Ensembl
chr6:6643278..6729025hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg3885748
hg1985748
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18144268
Samples
Known GenesLY86
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6396330
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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