A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3981789



Internal ID18858180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:7192373..7192973hg38UCSC Ensembl
Outerchr4:7194100..7194700hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1118996
Supporting Variants
SamplesKWS1
Known GenesSORCS2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3981789
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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