A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447427



Internal ID21104980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:35304278..35304608hg38UCSC Ensembl
chr10:35593206..35593536hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17980296
Samples
Known GenesCCNY
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447427
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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