A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14325900



Internal ID22261120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3195158..3195720hg38UCSC Ensembl
chr6:3195392..3195954hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38563
hg19563
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3526489
Supporting Variants
SamplesNA19238
Known GenesLOC100507194
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14325900
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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