A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3770008



Internal ID18958828
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 StatusS
Merged Variantsnsv1078828
Supporting Variants
SamplesKWP1
Known GenesZBTB7B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3770008
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer