A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1075527



Internal ID19322855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:8208677..8230378hg38UCSC Ensembl
chr8:8066199..8087900hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3821702
hg1921702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3769454
SamplesKWP1
Known GenesFAM86B3P
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1075527
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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