A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453294



Internal ID21110847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:102880962..103106641hg38UCSC Ensembl
chr9:105643244..105868923hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38225680
hg19225680
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18173646
Samples
Known GenesCYLC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453294
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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