A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6523948



Internal ID20897309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75896316..75907681hg38UCSC Ensembl
chr17:73892397..73903762hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3811366
hg1911366
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18038177
Samples
Known GenesMRPL38, TRIM65
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6523948
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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