A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1074341



Internal ID19321702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:167350767..167350974hg38UCSC Ensembl
chr5:166777772..166777979hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38208
hg19208
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3769352
SamplesKWP1
Known GenesTENM2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1074341
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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