A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156204



Internal ID22086709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:97251263..97263981hg38UCSC Ensembl
Outerchr4:97250644..97267978hg38UCSC Ensembl
Innerchr4:98172414..98185132hg19UCSC Ensembl
Outerchr4:98171795..98189129hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg3817335
hg1917335
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4015382, nssv4015381, nssv4014733, nssv4015378, nssv4015388, nssv4015384, nssv4015379, nssv4014731, nssv4014734, nssv4014732, nssv4015387, nssv4015386, nssv4015380, nssv4015389, nssv4015383, nssv4015385
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156204
Frequency
Sample Size131
Observed Gain1
Observed Loss15
Observed Complex0
Frequencyn/a


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