A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3962818



Internal ID19210133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:41199700..41199822hg38UCSC Ensembl
Outerchr15:41491898..41492020hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1129379
Supporting Variants
SamplesKWS1
Known GenesEXD1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3962818
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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