A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3204492



Internal ID22353333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73559736..73560177hg38UCSC Ensembl
chr6:74269459..74269900hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38442
hg19442
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14329408, nssv14329409
SamplesHG00731, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3204492
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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