A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057295



Internal ID19146514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:53368137..53445339hg38UCSC Ensembl
Innerchr19:53871390..53948592hg19UCSC Ensembl
Innerchr19:58563202..58640404hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3877203
hg1977203
hg1877203
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3646n100
Supporting Variantsnssv3573239
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)nsv1057295
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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