A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452635



Internal ID21110188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5771966..5772720hg38UCSC Ensembl
chr10:5813929..5814683hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38755
hg19755
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17983079
Samples
Known GenesGDI2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452635
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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