A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521888



Internal ID20895249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75452081..75453784hg38UCSC Ensembl
chr17:73448162..73449865hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg381704
hg191704
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18038152
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521888
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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