A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035226



Internal ID18777757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46536457..46588384hg38UCSC Ensembl
Innerchr10:46961233..47013160hg19UCSC Ensembl
Innerchr10:46381239..46433166hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3851928
hg1951928
hg1851928
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv771n100
Supporting Variantsnssv3503560
Samples
Known GenesGPRIN2, SYT15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035226
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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