A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334677



Internal ID20867864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:1500785..1530653hg38UCSC Ensembl
chr1:1436165..1466033hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3829869
hg1929869
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv24n223
Supporting Variantsnssv18201515
Samples
Known GenesATAD3A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334677
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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