A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510577



Internal ID20883897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85637408..85648482hg38UCSC Ensembl
chr16:85671014..85682088hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3811075
hg1911075
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188172
Samples
Known GenesGSE1, MIR7851
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510577
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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