A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2803558



Internal ID21248896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61273529..61273529hg38UCSC Ensembl
chr20:59848585..59848585hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13679161, nssv13686334
Samples
Known GenesCDH4
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2803558
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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