A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156537



Internal ID22086938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:76726442..76743087hg38UCSC Ensembl
Outerchr6:76720013..76751356hg38UCSC Ensembl
Innerchr6:77436159..77452804hg19UCSC Ensembl
Outerchr6:77429730..77461073hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3831344
hg1931344
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv252n97
Supporting Variantsnssv4021632, nssv4021633, nssv4021630, nssv4021629, nssv4021631
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156537
Frequency
Sample Size131
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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