A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1141898



Internal ID18914201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:92701962..92706899hg38UCSC Ensembl
Outerchr1:93167519..93172456hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg384938
hg194938
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3993405, nssv3987825
SamplesKWS1, KWS2
Known GenesEVI5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1141898
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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