A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1071513



Internal ID19320571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17245290..17246491hg38UCSC Ensembl
chr19:17356099..17357300hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg381202
hg191202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3761965
SamplesKWP1
Known GenesNR2F6
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1071513
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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