A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3516353



Internal ID18814634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:34167763..34189505hg38UCSC Ensembl
Innerchr10:34456691..34478433hg19UCSC Ensembl
Innerchr10:34496697..34518439hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3821743
hg1921743
hg1821743
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044684
Supporting Variants
Samples
Known GenesPARD3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3516353
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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