A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3978700



Internal ID19231912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:20672612..20672706hg38UCSC Ensembl
Outerchr16:20683934..20684028hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1116516
Supporting Variants
SamplesKWS2
Known GenesACSM1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3978700
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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