A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1071498



Internal ID18973315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3406342..3406527hg38UCSC Ensembl
chr19:3406340..3406525hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38186
hg19186
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3767085
SamplesKWP1
Known GenesNFIC
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1071498
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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