A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441727



Internal ID21099280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:35471356..35481120hg38UCSC Ensembl
chr10:35760284..35770048hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg389765
hg199765
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979385
Samples
Known GenesCCNY
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441727
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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