A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6397641



Internal ID21055194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87429244..87433587hg38UCSC Ensembl
chr6:88138962..88143305hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg384344
hg194344
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18149094
Samples
Known GenesC6orf165
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6397641
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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