A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18161902



Internal ID20728942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:88038001..88043200hg38UCSC Ensembl
chr7:87667316..87672515hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg385200
hg195200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6603724
Supporting Variants
Samples
Known GenesADAM22
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18161902
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00808


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