A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038243



Internal ID18780774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46401133..46560078hg38UCSC Ensembl
Innerchr10:46989539..47148630hg19UCSC Ensembl
Innerchr10:46409545..46568636hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38158946
hg19159092
hg18159092
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv781n100
Supporting Variantsnssv3705760
Samples
Known GenesGPRIN2, HNRNPA1P33, 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)nsv1038243
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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