A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516514



Internal ID20889875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:9569689..9570001hg38UCSC Ensembl
chr20:9550336..9550648hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18069238
Samples
Known GenesPAK7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516514
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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