A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6387773



Internal ID21045326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:7444366..7481513hg38UCSC Ensembl
chr5:7444479..7481626hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3837148
hg1937148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18132237
Samples
Known GenesADCY2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6387773
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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