A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3510599



Internal ID18808880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:121004150..121017973hg38UCSC Ensembl
Innerchr10:122763663..122777486hg19UCSC Ensembl
Innerchr10:122753653..122767476hg18UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg3813824
hg1913824
hg1813824
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048506
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)nssv3510599
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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