A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608887



Internal ID20981958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:99417725..99418958hg38UCSC Ensembl
chr6:99865601..99866834hg19UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg381234
hg191234
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231346
Samples
Known GenesPNISR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608887
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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