A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4021497



Internal ID22083128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:1696479..1720956hg38UCSC Ensembl
Outerchr1:1575421..1731499hg38UCSC Ensembl
Innerchr1:1627918..1652395hg19UCSC Ensembl
Outerchr1:1510801..1662938hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg38156079
hg19152138
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156357
Supporting Variants
Samples
Known GenesC1orf233, CDK11A, CDK11B, MIB2, MMP23A, MMP23B, SLC35E2, SLC35E2B
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4021497
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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