A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3960897



Internal ID19210861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:29877839..29906201hg38UCSC Ensembl
Outerchr4:29879461..29907823hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3828363
hg1928363
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1120141
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3960897
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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