A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155377



Internal ID22085882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25266637..25336853hg38UCSC Ensembl
Outerchr1:25256850..25346663hg38UCSC Ensembl
Innerchr1:25593128..25663344hg19UCSC Ensembl
Outerchr1:25583341..25673154hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3889814
hg1989814
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8n97
Supporting Variantsnssv4012209
Samples
Known GenesRHD, TMEM50A
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155377
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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