A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3989545



Internal ID19226877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:186627181..186627296hg38UCSC Ensembl
Outerchr4:187548335..187548450hg19UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1135947
Supporting Variants
SamplesKWS2
Known GenesFAT1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3989545
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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