A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067058



Internal ID19156277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:7162372..7266971hg38UCSC Ensembl
Innerchr19:7162383..7266982hg19UCSC Ensembl
Innerchr19:7113383..7217982hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38104600
hg19104600
hg18104600
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3423n100
Supporting Variantsnssv3564664
Samples
Known GenesINSR
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1067058
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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