A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18063986



Internal ID20631026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:7957488..7993119hg38UCSC Ensembl
chr1:8017548..8053179hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg3835632
hg1935632
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6318948
Supporting Variants
Samples
Known GenesPARK7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18063986
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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