A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3934577



Internal ID21354646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:239068848..239068945hg38UCSC Ensembl
chr2:239990544..239990641hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15178752
SamplesHG002
Known GenesHDAC4, MIR4440
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3934577
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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