A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1073056



Internal ID19323961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35226696..35227097hg38UCSC Ensembl
chr20:33814499..33814900hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3764071
SamplesKWP1
Known GenesMMP24
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1073056
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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