A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501989



Internal ID20875229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:33437076..33443627hg38UCSC Ensembl
chr17:31764094..31770645hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg386552
hg196552
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035619
Samples
Known GenesASIC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501989
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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