A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1072864



Internal ID18975949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14165387..14167988hg38UCSC Ensembl
chr19:14276199..14278800hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg382602
hg192602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3771505
SamplesKWP1
Known GenesLOC100507373, LPHN1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1072864
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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