A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058119



Internal ID18800650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:56197884..56233260hg38UCSC Ensembl
Innerchr19:56709253..56744629hg19UCSC Ensembl
Innerchr19:61401065..61436441hg18UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3835377
hg1935377
hg1835377
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3683n100
Supporting Variantsnssv3570447
Samples
Known GenesZSCAN5A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058119
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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