A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999134



Internal ID19158670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:27113679..27268878hg38UCSC Ensembl
Innerchr4:27115301..27270500hg19UCSC Ensembl
Innerchr4:26724399..26879598hg18UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38155200
hg19155200
hg18155200
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3737767
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)nsv999134
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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