A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045126



Internal ID18787657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46554143..46606240hg38UCSC Ensembl
Innerchr10:46943377..46995474hg19UCSC Ensembl
Innerchr10:46363383..46415480hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3852098
hg1952098
hg1852098
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv759n100
Supporting Variantsnssv3507943
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)nsv1045126
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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