A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155824



Internal ID22086329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:771719..915307hg38UCSC Ensembl
Outerchr1:690090..939522hg38UCSC Ensembl
Innerchr1:707099..850687hg19UCSC Ensembl
Outerchr1:625470..874902hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg38249433
hg19249433
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1n97
Supporting Variantsnssv4015239
Samples
Known GenesFAM41C, FAM87B, LINC00115, LINC01128, LOC100130417, LOC100133331, LOC100288069, SAMD11
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155824
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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