A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060009



Internal ID19149228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43208086..43249346hg38UCSC Ensembl
Innerchr19:43712238..43753498hg19UCSC Ensembl
Innerchr19:48404078..48445338hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3841261
hg1941261
hg1841261
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3600n100
Supporting Variantsnssv3573685, nssv3724863, nssv3573684, nssv3573681, nssv3573682, nssv3573683
Samples
Known GenesLOC284344
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060009
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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