A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6613959



Internal ID20987030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:136504591..136504968hg38UCSC Ensembl
chr6:136825729..136826106hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38378
hg19378
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216024
Samples
Known GenesMAP7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6613959
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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