A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064929



Internal ID18807460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:23376681..23644933hg38UCSC Ensembl
Innerchr19:23559483..23827735hg19UCSC Ensembl
Innerchr19:23351323..23619575hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38268253
hg19268253
hg18268253
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3724329
Samples
Known GenesZNF91
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064929
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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