A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042403



Internal ID19131622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:34771494..34859811hg38UCSC Ensembl
Innerchr10:35060422..35148739hg19UCSC Ensembl
Innerchr10:35100428..35188745hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3888318
hg1988318
hg1888318
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv704n100
Supporting Variantsnssv3506684
Samples
Known GenesPARD3, PARD3-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042403
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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