A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1109855



Internal ID19285114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:29525749..29525803hg38UCSC Ensembl
Outerchr7:29565365..29565419hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3958250
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1109855
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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