A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3510943



Internal ID18809224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:121004150..121030305hg38UCSC Ensembl
Innerchr10:122763663..122789818hg19UCSC Ensembl
Innerchr10:122753653..122779808hg18UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg3826156
hg1926156
hg1826156
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041174
Supporting Variants
Samples
Known GenesMIR5694
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3510943
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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