A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156538



Internal ID22086939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:76726442..76751356hg38UCSC Ensembl
Outerchr6:76720013..76758214hg38UCSC Ensembl
Innerchr6:77436159..77461073hg19UCSC Ensembl
Outerchr6:77429730..77467931hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3838202
hg1938202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv252n97
Supporting Variantsnssv4021635, nssv4021634
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156538
Frequency
Sample Size131
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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