A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057262



Internal ID19146481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:7168922..7245357hg38UCSC Ensembl
Innerchr19:7168933..7245368hg19UCSC Ensembl
Innerchr19:7119933..7196368hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3876436
hg1976436
hg1876436
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564665
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)nsv1057262
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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