A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18152711



Internal ID20719751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:128078059..128079318hg38UCSC Ensembl
chr7:127718111..127719370hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg381260
hg191260
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6432254
Supporting Variants
Samples
Known GenesSND1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18152711
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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