A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1077474



Internal ID18979009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:57436701..60345451hg38UCSC Ensembl
chr6:57301499..57317300hg19UCSC Ensembl
Cytoband6p11.2
Allele length
AssemblyAllele length
hg382908751
hg1915802
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3765198
SamplesKWP1
Known GenesPRIM2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1077474
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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