A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052787



Internal ID18795318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46428386..46481988hg38UCSC Ensembl
Innerchr10:47067469..47121369hg19UCSC Ensembl
Innerchr10:46487475..46541375hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3853603
hg1953901
hg1853901
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv814n100
Supporting Variantsnssv3521066, nssv3515166, nssv3507258
Samples
Known GenesLINC00842, 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)nsv1052787
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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