A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18138302



Internal ID20705342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:136638720..136639410hg38UCSC Ensembl
chr6:136959858..136960548hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38691
hg19691
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6617129
Supporting Variants
Samples
Known GenesMAP3K5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18138302
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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