A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3768314



Internal ID19306455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68132361..68136588hg38UCSC Ensembl
chr15:68424699..68428926hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg384228
hg194228
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1069599
Supporting Variants
SamplesKWP1
Known GenesPIAS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3768314
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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