A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3772062



Internal ID19314554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:73093064..73093565hg38UCSC Ensembl
chr8:74005299..74005800hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1075146
Supporting Variants
SamplesKWP1
Known GenesSBSPON
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3772062
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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