A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156526



Internal ID22086927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:73290632..73298260hg38UCSC Ensembl
Outerchr6:73288278..73309615hg38UCSC Ensembl
Innerchr6:74000355..74007983hg19UCSC Ensembl
Outerchr6:73998001..74019338hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3821338
hg1921338
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4019852
Samples
Known GenesC6orf147, KHDC1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156526
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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