A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1073940



Internal ID18970157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:177370498..177371299hg38UCSC Ensembl
chr5:176797499..176798300hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38802
hg19802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3772912
SamplesKWP1
Known GenesRGS14
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1073940
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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