A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1074443



Internal ID19324986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:161090701..161090930hg38UCSC Ensembl
chr6:161511733..161511962hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38230
hg19230
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3771330
SamplesKWP1
Known GenesMAP3K4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1074443
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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