A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060229



Internal ID19149448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:53373607..53445339hg38UCSC Ensembl
Innerchr19:53876860..53948592hg19UCSC Ensembl
Innerchr19:58568672..58640404hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3871733
hg1971733
hg1871733
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3646n100
Supporting Variantsnssv3726523, nssv3573240
Samples
Known GenesTPM3P9, ZNF525, ZNF761, ZNF765
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060229
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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