A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059568



Internal ID18802099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:36315573..36356962hg38UCSC Ensembl
Innerchr19:36806475..36847864hg19UCSC Ensembl
Innerchr19:41498315..41539704hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3841390
hg1941390
hg1841390
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3524n100
Supporting Variantsnssv3568180
Samples
Known GenesLINC00665, ZFP14
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059568
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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