A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1148609



Internal ID19200514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:39096106..39096371hg38UCSC Ensembl
Outerchr8:38953625..38953890hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38266
hg19266
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4000645
SamplesKWB1
Known GenesADAM9
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1148609
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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