A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1075177



Internal ID19318069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:142501646..142501896hg38UCSC Ensembl
chr8:143583007..143583257hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38251
hg19251
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3763238
SamplesKWP1
Known GenesBAI1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1075177
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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