A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18153359



Internal ID20720399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:129347614..129348335hg38UCSC Ensembl
chr7:128987455..128988176hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg38722
hg19722
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6428230
Supporting Variants
Samples
Known GenesAHCYL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18153359
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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