A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3525806



Internal ID22395184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:29183991..29184287hg38UCSC Ensembl
chr1:29510503..29510799hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14358985, nssv14358984
SamplesHG00731, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3525806
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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