A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3962777



Internal ID18868641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:25287254..25287800hg38UCSC Ensembl
Outerchr1:25613745..25614291hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38547
hg19547
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1116486
Supporting Variants
SamplesKWS1
Known GenesRHD
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3962777
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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