A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506722



Internal ID20880006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:1616656..1694931hg38UCSC Ensembl
chr16:1666657..1744932hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3878276
hg1978276
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193385
Samples
Known GenesCRAMP1L, HN1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506722
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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