A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6433127



Internal ID21090680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39260001..39439900hg38UCSC Ensembl
chr8:39117520..39297419hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38179900
hg19179900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223547
Samples
Known GenesADAM32, ADAM5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6433127
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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