A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321142



Internal ID20854245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:67742295..67755509hg38UCSC Ensembl
chr1:68207978..68221192hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3813215
hg1913215
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204317
Samples
Known GenesGNG12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321142
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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