A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18200922



Internal ID20767962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156291691..156308597hg38UCSC Ensembl
chr1:156261482..156278388hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg3816907
hg1916907
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6328648
Supporting Variants
Samples
Known GenesC1orf85, TMEM79, VHLL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18200922
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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