A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610921



Internal ID20983992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:79457359..79457548hg38UCSC Ensembl
chr7:79086675..79086864hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38190
hg19190
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18159025
Samples
Known GenesMAGI2-AS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610921
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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