A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1125345



Internal ID19265934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:71061447..71061541hg38UCSC Ensembl
Outerchr12:71455227..71455321hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3983521
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1125345
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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