A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508485



Internal ID20881786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:7139001..7143600hg38UCSC Ensembl
chr17:7042320..7046919hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg384600
hg194600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184017
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508485
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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