A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520542



Internal ID20893903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:73336686..73337481hg38UCSC Ensembl
chr17:71332825..71333620hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38796
hg19796
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18038364
Samples
Known GenesSDK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520542
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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