A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18060067



Internal ID20627107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:38877015..38878980hg38UCSC Ensembl
chr1:39342687..39344652hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg381966
hg191966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6331148
Supporting Variants
Samples
Known GenesGJA9, GJA9-MYCBP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18060067
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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