A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1120885



Internal ID18936372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:104774128..104774393hg38UCSC Ensembl
Outerchr6:105222003..105222268hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg38266
hg19266
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3355n106
Supporting Variantsnssv3963333
SamplesKWS2
Known GenesHACE1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1120885
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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