A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1070270



Internal ID18970951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43577801..43651202hg38UCSC Ensembl
chr15:43869999..43943400hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg3873402
hg1973402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3770762
SamplesKWP1
Known GenesCATSPER2, CKMT1B, PPIP5K1, RNU6-28P, STRC
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1070270
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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