A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18159592



Internal ID20726632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:79007301..79008400hg38UCSC Ensembl
chr7:78636617..78637716hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6611142
Supporting Variants
Samples
Known GenesMAGI2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18159592
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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