A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6425727



Internal ID21083280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:30197700..30502690hg38UCSC Ensembl
chr9:30197698..30502688hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38304991
hg19304991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7681n223
Supporting Variantsnssv18191295
Samples
Known GenesLOC401497
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6425727
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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