A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3765378



Internal ID19313392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:115686924..115690318hg38UCSC Ensembl
chr1:116229545..116232939hg19UCSC Ensembl
Cytoband1p13.1
Allele length
AssemblyAllele length
hg383395
hg193395
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1077565
Supporting Variants
SamplesKWP1
Known GenesVANGL1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3765378
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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