A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18063534



Internal ID20630574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:6979903..6987835hg38UCSC Ensembl
chr1:7039963..7047895hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg387933
hg197933
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6327496
Supporting Variants
Samples
Known GenesCAMTA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18063534
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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