A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007053



Internal ID19096271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:22571911..22656494hg38UCSC Ensembl
Innerchr4:22573534..22658117hg19UCSC Ensembl
Innerchr4:22182632..22267215hg18UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3884584
hg1984584
hg1884584
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3620581
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007053
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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