A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504856



Internal ID20878120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:8679889..8680915hg38UCSC Ensembl
chr17:8583207..8584233hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg381027
hg191027
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18039082
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504856
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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