A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156274



Internal ID22084750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:177546882..177565452hg38UCSC Ensembl
Outerchr4:177543915..177574437hg38UCSC Ensembl
Innerchr4:178468036..178486606hg19UCSC Ensembl
Outerchr4:178465069..178495591hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg3830523
hg1930523
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4019397
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156274
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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