A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510632



Internal ID20883953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:61459288..61459857hg38UCSC Ensembl
chr16:61493192..61493761hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38570
hg19570
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18030752
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510632
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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