A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352714



Internal ID21010267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:68136268..68136653hg38UCSC Ensembl
chr2:68363400..68363785hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg38386
hg19386
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206972
Samples
Known GenesWDR92
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352714
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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