A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6354304



Internal ID21011857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:77936973..77998284hg38UCSC Ensembl
chr2:78164099..78225410hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3861312
hg1961312
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3933n223
Supporting Variantsnssv18207679
Samples
Known GenesSNAR-H
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6354304
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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