A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526200



Internal ID22395580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:228894571..228895191hg38UCSC Ensembl
chr2:229759287..229759907hg19UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg38621
hg19621
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14298235, nssv14298234
SamplesHG00732, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526200
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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