A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3521736



Internal ID18820017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:52761330..52802372hg38UCSC Ensembl
Innerchr10:54521090..54562132hg19UCSC Ensembl
Innerchr10:54191096..54232138hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3841043
hg1941043
hg1841043
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1051777
Supporting Variants
Samples
Known GenesMBL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3521736
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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