A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001959



Internal ID19091176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:145907227..145944673hg38UCSC Ensembl
Innerchr3:145625014..145662460hg19UCSC Ensembl
Innerchr3:147107704..147145150hg18UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3837447
hg1937447
hg1837447
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4917n100
Supporting Variantsnssv3606141, nssv3606142
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)nsv1001959
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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