A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504158



Internal ID20877419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:30275801..30302600hg38UCSC Ensembl
chr16:30287122..30313921hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3826800
hg1926800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186324
Samples
Known GenesLOC440354, LOC595101
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504158
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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