A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3735243



Internal ID19033524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:104481103..104718359hg38UCSC Ensembl
Innerchr3:104199947..104437203hg19UCSC Ensembl
Innerchr3:105682637..105919893hg18UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38237257
hg19237257
hg18237257
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1000438
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)nssv3735243
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer