A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616763



Internal ID20989834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:136359101..136365600hg38UCSC Ensembl
chr6:136680239..136686738hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg386500
hg196500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216022
Samples
Known GenesMAP7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616763
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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