A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057897



Internal ID19147116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:46190144..46275270hg38UCSC Ensembl
Innerchr19:46693401..46778527hg19UCSC Ensembl
Innerchr19:51385241..51470367hg18UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3885127
hg1985127
hg1885127
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3607n100
Supporting Variantsnssv3573801
Samples
Known GenesDKFZp434J0226, IGFL1, RNU6-66P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057897
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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