A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319960



Internal ID20853057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:7374898..7395645hg38UCSC Ensembl
chr1:7434959..7455705hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg3820748
hg1920747
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18063839
Samples
Known GenesCAMTA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319960
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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