A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156530



Internal ID22086931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:73999993..74007305hg38UCSC Ensembl
Outerchr6:73997661..74009077hg38UCSC Ensembl
Innerchr6:74709709..74717021hg19UCSC Ensembl
Outerchr6:74707377..74718793hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3811417
hg1911417
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4021613, nssv4021616, nssv4021617, nssv4021618, nssv4021612, nssv4021614, nssv4021615
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156530
Frequency
Sample Size131
Observed Gain6
Observed Loss1
Observed Complex0
Frequencyn/a


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