A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18062032



Internal ID20629072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:60002366..60008468hg38UCSC Ensembl
chr1:60468038..60474140hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg386103
hg196103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6325042
Supporting Variants
Samples
Known GenesC1orf87
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18062032
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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