A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6388272



Internal ID21045825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:7666313..7674946hg38UCSC Ensembl
chr5:7666426..7675059hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg388634
hg198634
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18134491
Samples
Known GenesADCY2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6388272
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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