A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4019397



Internal ID22081028
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 Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156274
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4019397
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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