A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1070742



Internal ID18974687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:8564216..8564305hg38UCSC Ensembl
chr16:8614218..8614307hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3771261
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1070742
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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