A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3978960



Internal ID19230920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:2542243..2659155hg38UCSC Ensembl
Outerchr16:2592244..2709156hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38116913
hg19116913
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1140247
Supporting Variants
SamplesKWS2
Known GenesERVK13-1, FLJ42627, LOC652276, PDPK1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3978960
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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