A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156548



Internal ID22086949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:78811345..78818857hg38UCSC Ensembl
Outerchr6:78810972..78821538hg38UCSC Ensembl
Innerchr6:79521062..79528574hg19UCSC Ensembl
Outerchr6:79520689..79531255hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3810567
hg1910567
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4021700, nssv4021702, nssv4021687, nssv4021708, nssv4021690, nssv4021723, nssv4021714, nssv4021717, nssv4021722, nssv4021694, nssv4021703, nssv4021695, nssv4021697, nssv4021712, nssv4021705, nssv4021691, nssv4021713, nssv4021719, nssv4021698, nssv4021707, nssv4021686, nssv4021704, nssv4021720, nssv4021688, nssv4021721, nssv4021724, nssv4021710, nssv4021725, nssv4021692, nssv4021718, nssv4021709, nssv4021727, nssv4021701, nssv4021696, nssv4021711, nssv4021726, nssv4021689, nssv4021699, nssv4021715, nssv4021716, nssv4021706, nssv4021693
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156548
Frequency
Sample Size131
Observed Gain0
Observed Loss42
Observed Complex0
Frequencyn/a


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