A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3987801



Internal ID19206778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:9304388..9427640hg38UCSC Ensembl
Outerchr12:9456984..9580236hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38123253
hg19123253
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1133004
Supporting Variants
SamplesKWS1
Known GenesDDX12P, LOC642846
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3987801
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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