A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514167



Internal ID20887519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:70625857..70691874hg38UCSC Ensembl
chr16:70659760..70725777hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3866018
hg1966018
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18031915
Samples
Known GenesIL34, MTSS1L, VAC14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514167
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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