A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1074696



Internal ID19322622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:16226076..16226777hg38UCSC Ensembl
chr4:16227699..16228400hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg38702
hg19702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3767887
SamplesKWP1
Known GenesTAPT1, TAPT1-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1074696
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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