A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3611337



Internal ID18909618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:191602847..191861798hg38UCSC Ensembl
Innerchr3:191320636..191579587hg19UCSC Ensembl
Innerchr3:192803330..193062281hg18UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg38258952
hg19258952
hg18258952
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1001082
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3611337
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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