A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532048



Internal ID20905409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75068478..75070734hg38UCSC Ensembl
chr17:73064573..73066829hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg382257
hg192257
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037484
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532048
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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