A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3611388



Internal ID18562983
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 StatusS
Merged Variantsnsv1013035
Supporting Variants
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)nssv3611388
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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