A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3985066



Internal ID18864256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:69598014..69598814hg38UCSC Ensembl
Outerchr7:69063000..69063800hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg38801
hg19801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1126793
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3985066
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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