A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3200101



Internal ID22349600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:44289976..44367268hg38UCSC Ensembl
chr4:44291993..44369285hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3877293
hg1977293
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6569n152
Supporting Variantsnssv14313180
SamplesHG00512
Known GenesKCTD8
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3200101
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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