A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3934624



Internal ID21354694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:88736195..88736525hg38UCSC Ensembl
chr5:88032012..88032342hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15196371
SamplesHG002
Known GenesMEF2C
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3934624
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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