A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155792



Internal ID22086297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:34637053..34638890hg38UCSC Ensembl
Outerchr1:34626073..34648667hg38UCSC Ensembl
Innerchr1:35102654..35104491hg19UCSC Ensembl
Outerchr1:35091674..35114268hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3822595
hg1922595
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4015221, nssv4013639, nssv4015223, nssv4012338, nssv4015195, nssv4015219, nssv4015220, nssv4015222, nssv4012216, nssv4015094, nssv4013437, nssv4012217, nssv4015225, nssv4012237, nssv4015218, nssv4013538, nssv4015224
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155792
Frequency
Sample Size131
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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