A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18147501



Internal ID20714541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73482901..73483800hg38UCSC Ensembl
chr6:74192624..74193523hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6411173
Supporting Variants
Samples
Known GenesMTO1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18147501
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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