A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1073814



Internal ID18974504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:168155448..168156349hg38UCSC Ensembl
chr4:169076599..169077500hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38902
hg19902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3764903
SamplesKWP1
Known GenesANXA10
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1073814
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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