A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441893



Internal ID21099446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:95540203..95547539hg38UCSC Ensembl
chr10:97299960..97307296hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg387337
hg197337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985743
Samples
Known GenesSORBS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441893
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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