A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3521039



Internal ID18819320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:122380682..122437149hg38UCSC Ensembl
Innerchr10:124140198..124196665hg19UCSC Ensembl
Innerchr10:124130188..124186655hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3856468
hg1956468
hg1856468
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050574
Supporting Variants
Samples
Known GenesMIR3941, PLEKHA1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3521039
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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