A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3979014



Internal ID19245625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:51409039..51409095hg38UCSC Ensembl
Outerchr15:51701236..51701292hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1140305
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3979014
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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