A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435904



Internal ID21093457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:70237849..70244123hg38UCSC Ensembl
chr9:72852765..72859039hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg386275
hg196275
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179445
Samples
Known GenesSMC5-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435904
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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