A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3961295



Internal ID19223827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:232792392..232792454hg38UCSC Ensembl
Outerchr1:232928138..232928200hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1110883
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3961295
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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