A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045977



Internal ID18788508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46428386..46481242hg38UCSC Ensembl
Innerchr10:47068215..47121369hg19UCSC Ensembl
Innerchr10:46488221..46541375hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3852857
hg1953155
hg1853155
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv815n100
Supporting Variantsnssv3519401, nssv3705906, nssv3517303, nssv3514797, nssv3512899, nssv3507197, nssv3519194, nssv3508583
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)nsv1045977
Frequency
Sample Size29084
Observed Gain7
Observed Loss1
Observed Complex0
Frequencyn/a


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