A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1077843



Internal ID18970875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:45512133..45519934hg38UCSC Ensembl
chr17:43589499..43597300hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg387802
hg197802
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3763970
SamplesKWP1
Known GenesLRRC37A4P
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1077843
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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