A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1078828



Internal ID18977061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155000023..155003124hg38UCSC Ensembl
chr1:154972499..154975600hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg383102
hg193102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3770008
SamplesKWP1
Known GenesZBTB7B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1078828
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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