A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3974782



Internal ID18900070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:70938718..70938778hg38UCSC Ensembl
Outerchr4:71804435..71804495hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1136873
Supporting Variants
SamplesKWS2
Known GenesMOB1B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3974782
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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