A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517363



Internal ID20890724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76015703..76017380hg38UCSC Ensembl
chr17:74011784..74013461hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg381678
hg191678
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18038186
Samples
Known GenesEVPL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517363
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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