A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951696



Internal ID17300570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:1011601..1033700hg38UCSC Ensembl
Outerchr8:961601..983700hg19UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg3822100
hg1922100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998673
SamplesBILGI_BIOE
Known GenesERICH1-AS1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951696
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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