A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv957864



Internal ID17306737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:24193854..24197192hg38UCSC Ensembl
Outerchr1:24520344..24523682hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg383339
hg193339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1n73
Supporting Variantsnssv3005071
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv957864
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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