A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064851



Internal ID18807382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:36419357..37198819hg38UCSC Ensembl
Innerchr19:36910259..37689721hg19UCSC Ensembl
Innerchr19:41602099..42381561hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38779463
hg19779463
hg18779463
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3568185
Samples
Known GenesLOC644189, LOC728752, ZNF260, ZNF345, ZNF382, ZNF420, ZNF461, ZNF529, ZNF566, ZNF567, ZNF568, ZNF585A, ZNF585B, ZNF790, ZNF790-AS1, ZNF829, ZNF850
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064851
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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