A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617798



Internal ID20990869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:165289001..165290300hg38UCSC Ensembl
chr6:165702490..165703789hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18142391
Samples
Known GenesC6orf118
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617798
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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