A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3519066



Internal ID18817347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:45529172..45592613hg38UCSC Ensembl
Innerchr10:46024620..46088061hg19UCSC Ensembl
Innerchr10:45344626..45408067hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3863442
hg1963442
hg1863442
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052233
Supporting Variants
Samples
Known GenesMARCH8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3519066
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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