A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6523047



Internal ID20896408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36877108..36878303hg38UCSC Ensembl
chr20:35505511..35506706hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg381196
hg191196
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068077
Samples
Known GenesTLDC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6523047
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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