A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18136961



Internal ID20704001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:10786211..10786806hg38UCSC Ensembl
chr6:10786444..10787039hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg38596
hg19596
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6411995
Supporting Variants
Samples
Known GenesMAK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18136961
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00049


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