A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499029



Internal ID20872245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:27222157..27225258hg38UCSC Ensembl
chr16:27233478..27236579hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg383102
hg193102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029267
Samples
Known GenesNSMCE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499029
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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