A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156067



Internal ID22086572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:77272697..77285823hg38UCSC Ensembl
Outerchr1:77265734..77286937hg38UCSC Ensembl
Innerchr1:77738382..77751508hg19UCSC Ensembl
Outerchr1:77731419..77752622hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3821204
hg1921204
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4017905
Samples
Known GenesAK5
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156067
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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