A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522852



Internal ID20896213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:10063192..10074483hg38UCSC Ensembl
chr20:10043840..10055131hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg3811292
hg1911292
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18066214
Samples
Known GenesSNAP25-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522852
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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