A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3772178



Internal ID18968706
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 StatusS
Merged Variantsnsv1074465
Supporting Variants
SamplesKWP1
Known GenesSUN1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3772178
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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