A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436636



Internal ID21094189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:95752501..95754100hg38UCSC Ensembl
chr10:97512258..97513857hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985303
Samples
Known GenesENTPD1, ENTPD1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436636
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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