A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3960929



Internal ID19208600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:102423789..102442041hg38UCSC Ensembl
Outerchr8:103436017..103454269hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3818253
hg1918253
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1120168
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3960929
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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