A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18062948



Internal ID20629988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:7493441..7511466hg38UCSC Ensembl
chr1:7553501..7571526hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg3818026
hg1918026
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6329495
Supporting Variants
Samples
Known GenesCAMTA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18062948
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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