A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3765954



Internal ID19306312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:49096586..49096835hg38UCSC Ensembl
chr8:50009145..50009394hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg38250
hg19250
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1076082
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3765954
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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