A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18038208



Internal ID20605248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76282459..76288977hg38UCSC Ensembl
chr17:74278540..74285058hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg386519
hg196519
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6535157
Supporting Variants
Samples
Known GenesQRICH2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18038208
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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