A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531727



Internal ID20905088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:62406471..62417664hg38UCSC Ensembl
chr17:60483832..60495025hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg3811194
hg1911194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037176
Samples
Known GenesEFCAB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531727
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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