A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061027



Internal ID19150246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42816973..43252073hg38UCSC Ensembl
Innerchr19:43321125..43756225hg19UCSC Ensembl
Innerchr19:48012965..48448065hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38435101
hg19435101
hg18435101
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3572n100
Supporting Variantsnssv3723023, nssv3723022
Samples
Known GenesLOC100289650, LOC284344, PSG1, PSG10P, PSG11, PSG2, PSG4, PSG5, 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)nsv1061027
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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