A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1073264



Internal ID18974990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:178759776..178759946hg38UCSC Ensembl
chr3:178477564..178477734hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg38171
hg19171
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3770512
SamplesKWP1
Known GenesKCNMB2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1073264
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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