A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6341763



Internal ID20999316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:38727301..38741600hg38UCSC Ensembl
chr2:38954443..38968742hg19UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg3814300
hg1914300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3839n223
Supporting Variantsnssv18206931
Samples
Known GenesGALM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6341763
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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