A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6466623



Internal ID21124176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:78165151..78166435hg38UCSC Ensembl
chr11:77876197..77877481hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg381285
hg191285
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994183
Samples
Known GenesKCTD21-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6466623
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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