A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044357



Internal ID19133576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:47022685..47100644hg19UCSC Ensembl
Innerchr10:46442691..46520650hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg1977960
hg1877960
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv791n100
Supporting Variantsnssv3511758, nssv3705772
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)nsv1044357
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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