A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv625365



Internal ID15502212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31471963..31472911hg38UCSC Ensembl
Outerchr6:31471780..31473572hg38UCSC Ensembl
Innerchr6:31439740..31440688hg19UCSC Ensembl
Outerchr6:31439557..31441349hg19UCSC Ensembl
Innerchr6:31547719..31548667hg18UCSC Ensembl
Outerchr6:31547536..31549328hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg381793
hg191793
hg181793
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv511312
Supporting Variants
Samples1
Known GenesHCG26
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv625365
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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