A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007906



Internal ID19097125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:34425474..34565973hg38UCSC Ensembl
Innerchr3:34466966..34607465hg19UCSC Ensembl
Innerchr3:34441970..34582469hg18UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38140500
hg19140500
hg18140500
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3589591
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)nsv1007906
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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