A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004455



Internal ID19093673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:154903883..154971490hg38UCSC Ensembl
Innerchr3:154621672..154689279hg19UCSC Ensembl
Innerchr3:156104366..156171973hg18UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3867608
hg1967608
hg1867608
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3606352
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)nsv1004455
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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