A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155131



Internal ID22085636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:1696479..1741164hg38UCSC Ensembl
Outerchr1:1575421..1756148hg38UCSC Ensembl
Innerchr1:1627918..1672603hg19UCSC Ensembl
Outerchr1:1510801..1687587hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg38180728
hg19176787
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2n97
Supporting Variantsnssv4021549, nssv4009655, nssv4007065, nssv4004841, nssv4022617, nssv4023088, nssv4007054, nssv4007275
Samples
Known GenesC1orf233, CDK11A, CDK11B, MIB2, MMP23A, MMP23B, NADK, SLC35E2, SLC35E2B
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155131
Frequency
Sample Size131
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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