A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203662



Internal ID20770702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:6258028..6295606hg38UCSC Ensembl
chr1:6318088..6355666hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg3837579
hg1937579
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6316711
Supporting Variants
Samples
Known GenesACOT7, GPR153
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203662
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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