A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449731



Internal ID21107284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:99707696..99708159hg38UCSC Ensembl
chr10:101467453..101467916hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38464
hg19464
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985877
Samples
Known GenesENTPD7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449731
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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