A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063010



Internal ID19152229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42798345..43038667hg38UCSC Ensembl
Innerchr19:43302497..43542819hg19UCSC Ensembl
Innerchr19:47994337..48234659hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38240323
hg19240323
hg18240323
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3558n100
Supporting Variantsnssv3722975, nssv3569556, nssv3722976
Samples
Known GenesLOC100289650, PSG1, PSG10P, PSG11, PSG6, PSG7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063010
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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