A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1078355



Internal ID18974879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:39081127..39082428hg38UCSC Ensembl
chr1:39546799..39548100hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg381302
hg191302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3766295
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1078355
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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