A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415714



Internal ID21073267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:30698215..30793996hg38UCSC Ensembl
chr9:30698213..30793994hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3895782
hg1995782
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195481
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415714
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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