A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1077064



Internal ID18976179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:119887059..119887560hg38UCSC Ensembl
chr8:120899299..120899800hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3761969
SamplesKWP1
Known GenesDEPTOR
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1077064
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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