A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18062215



Internal ID20629255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:6235301..6236400hg38UCSC Ensembl
chr1:6295361..6296460hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6335253
Supporting Variants
Samples
Known GenesICMT, LINC00337
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18062215
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.073


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