A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1075557



Internal ID18969563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:70403064..70403965hg38UCSC Ensembl
chr8:71315299..71316200hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg38902
hg19902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3763475
SamplesKWP1
Known GenesNCOA2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1075557
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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