A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3982206



Internal ID19211921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:4681869..4682569hg38UCSC Ensembl
Outerchr7:4721500..4722200hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1145124
Supporting Variants
SamplesKWS1
Known GenesFOXK1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3982206
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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