A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500952



Internal ID20874182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:8320672..8345659hg38UCSC Ensembl
chr17:8223990..8248977hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3824988
hg1924988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18038804
Samples
Known GenesARHGEF15, ODF4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500952
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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