A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18060595



Internal ID20627635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26549339..26559818hg38UCSC Ensembl
chr1:26875830..26886309hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3810480
hg1910480
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6328040
Supporting Variants
Samples
Known GenesMIR1976, RPS6KA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18060595
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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