A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6336734



Internal ID20994287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:88739501..88795200hg38UCSC Ensembl
chr2:89039018..89094717hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg3855700
hg1955700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3974n223
Supporting Variantsnssv18207181
Samples
Known GenesANKRD36BP2, RPIA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6336734
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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