A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057700



Internal ID18800231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:30343427..31000378hg38UCSC Ensembl
Innerchr19:30834334..31491284hg19UCSC Ensembl
Innerchr19:35526174..36183124hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38656952
hg19656951
hg18656951
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3566568
Samples
Known GenesZNF536
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057700
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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