A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18201334



Internal ID20768374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:44077133..44143769hg38UCSC Ensembl
chr1:44542805..44609441hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg3866637
hg1966637
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6323715
Supporting Variants
Samples
Known GenesKLF17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18201334
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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