A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511989



Internal ID20885319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:29634584..29635435hg38UCSC Ensembl
chr17:27961602..27962453hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38852
hg19852
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18034712
Samples
Known GenesSSH2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511989
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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