A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510496



Internal ID20883815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88099137..88235310hg38UCSC Ensembl
chr16:88132743..88268916hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38136174
hg19136174
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193010
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510496
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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