A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6350090



Internal ID21007643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:216241518..216280130hg38UCSC Ensembl
chr2:217106241..217144853hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg3838613
hg1938613
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208181
Samples
Known GenesMARCH4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6350090
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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