A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063835



Internal ID18806366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:58473466..58586475hg38UCSC Ensembl
Innerchr19:58984833..59097842hg19UCSC Ensembl
Innerchr19:63676645..63789654hg18UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38113010
hg19113010
hg18113010
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3687n100
Supporting Variantsnssv3570460
Samples
Known GenesCENPBD1P1, CHMP2A, LOC100131691, MIR6807, MZF1, SLC27A5, TRIM28, UBE2M, ZBTB45, ZNF324, ZNF446
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063835
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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