A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515602



Internal ID20888963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:7608414..7609678hg38UCSC Ensembl
chr19:7673300..7674564hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381265
hg191265
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18049771
Samples
Known GenesCAMSAP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515602
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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