A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455587



Internal ID21113140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:48893721..48894969hg38UCSC Ensembl
chr10:50101766..50103014hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg381249
hg191249
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17980000
Samples
Known GenesWDFY4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455587
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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