A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321502



Internal ID20854608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:182417472..182418695hg38UCSC Ensembl
chr1:182386607..182387830hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg381224
hg191224
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201741
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321502
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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