A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18134520



Internal ID20701560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:7737601..7739900hg38UCSC Ensembl
chr5:7737714..7740013hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6395541
Supporting Variants
Samples
Known GenesADCY2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18134520
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00057


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