A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038700



Internal ID18781231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46402445..46469221hg38UCSC Ensembl
Innerchr10:47080230..47147302hg19UCSC Ensembl
Innerchr10:46500236..46567308hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3866777
hg1967073
hg1867073
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv812n100
Supporting Variantsnssv3510354
Samples
Known GenesHNRNPA1P33, LINC00842, LOC100996758, NPY4R
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038700
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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