A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3994787



Internal ID18863552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:3765773..3766673hg38UCSC Ensembl
Outerchr4:3767500..3768400hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38901
hg19901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1133576
Supporting Variants
SamplesKWS1
Known GenesADRA2C
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3994787
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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