A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18038374



Internal ID20605414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:73558404..73560380hg38UCSC Ensembl
chr17:71554543..71556519hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg381977
hg191977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6523835
Supporting Variants
Samples
Known GenesSDK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18038374
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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