A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510950



Internal ID20884274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66701501..66706200hg38UCSC Ensembl
chr16:66735404..66740103hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg384700
hg194700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2907n223
Supporting Variantsnssv18031304
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510950
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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