A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1074633



Internal ID19325384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:150762512..150763913hg38UCSC Ensembl
chr3:150480299..150481700hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg381402
hg191402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3770021
SamplesKWP1
Known GenesSIAH2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1074633
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