A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626049



Internal ID15502896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46441715..46489856hg38UCSC Ensembl
Outerchr10:46440412..46489856hg38UCSC Ensembl
Innerchr10:47058640..47108045hg19UCSC Ensembl
Outerchr10:47058530..47109348hg19UCSC Ensembl
Innerchr10:46478646..46528051hg18UCSC Ensembl
Outerchr10:46478536..46529354hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3849445
hg1950819
hg1850819
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv511437
Supporting Variants
Samples1
Known GenesLINC00842, LOC100996758, NPY4R
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv626049
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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