A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3202072



Internal ID22351280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:108753707..108754047hg38UCSC Ensembl
chr4:109674863..109675203hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38341
hg19341
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14316937
SamplesHG00733
Known GenesETNPPL
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3202072
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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