A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058527



Internal ID19147746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:7168922..7272690hg38UCSC Ensembl
Innerchr19:7168933..7272701hg19UCSC Ensembl
Innerchr19:7119933..7223701hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38103769
hg19103769
hg18103769
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3423n100
Supporting Variantsnssv3564666, nssv3564667
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)nsv1058527
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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