A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1146204



Internal ID19199847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:73711555..73711858hg38UCSC Ensembl
Outerchr6:74421278..74421581hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3999407
SamplesKWB1
Known GenesCD109
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1146204
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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