A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6331576



Internal ID20864740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:244352188..244392089hg38UCSC Ensembl
chr1:244515490..244555391hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3839902
hg1939902
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200658
Samples
Known GenesC1orf100
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6331576
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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