A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1074465



Internal ID18975825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:815862..817463hg38UCSC Ensembl
chr7:855499..857100hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg381602
hg191602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3772178
SamplesKWP1
Known GenesSUN1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1074465
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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