A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608072



Internal ID20981143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:120839903..120840249hg38UCSC Ensembl
chr7:120479957..120480303hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg38347
hg19347
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18151147
Samples
Known GenesTSPAN12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608072
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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