A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156572



Internal ID22086973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:112215137..112400042hg38UCSC Ensembl
Outerchr6:112208227..112400944hg38UCSC Ensembl
Innerchr6:112536338..112721244hg19UCSC Ensembl
Outerchr6:112529428..112722146hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38192718
hg19192719
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4022622
Samples
Known GenesLAMA4, RFPL4B
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156572
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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