A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3960802



Internal ID19205857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:22709967..22741103hg38UCSC Ensembl
Outerchr3:22751458..22782594hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3831137
hg1931137
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1120060
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3960802
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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