A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509277



Internal ID20882586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2909491..3033519hg38UCSC Ensembl
chr16:2959492..3083520hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38124029
hg19124029
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194272
Samples
Known GenesCCDC64B, CLDN6, CLDN9, FLYWCH1, HCFC1R1, KREMEN2, LINC00514, LOC100128770, PAQR4, PKMYT1, THOC6, TNFRSF12A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509277
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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