A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511377



Internal ID15850802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:156594543..156601615hg38UCSC Ensembl
Outerchr7:156590543..156602801hg38UCSC Ensembl
Innerchr7:156387237..156394309hg19UCSC Ensembl
Outerchr7:156383237..156395495hg19UCSC Ensembl
Innerchr7:156079998..156087070hg18UCSC Ensembl
Outerchr7:156075998..156088256hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3812259
hg1912259
hg1812259
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv625983
Samples1
Known GenesLINC01006
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511377
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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