A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3525568



Internal ID22394946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:173044551..173044605hg38UCSC Ensembl
chr4:173965702..173965756hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14317272, nssv14317271, nssv14317273
SamplesHG00731, HG00732, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3525568
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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