A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013035



Internal ID18755566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:195549241..195720039hg38UCSC Ensembl
Innerchr3:195276060..195446910hg19UCSC Ensembl
Innerchr3:196757349..196932581hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38170799
hg19170851
hg18175233
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5015n100
Supporting Variantsnssv3611389, nssv3611388
Samples
Known GenesAPOD, MIR570, SDHAP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013035
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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