A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18034754



Internal ID20601794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:30405501..30406400hg38UCSC Ensembl
chr17:28732519..28733418hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6500130
Supporting Variants
Samples
Known GenesCPD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18034754
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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