A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3962756



Internal ID18869541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:29512272..30672177hg38UCSC Ensembl
Outerchr10:29801201..30961106hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg381159906
hg191159906
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1129323
Supporting Variants
SamplesKWS1
Known GenesKIAA1462, LYZL2, MAP3K8, MIR604, MIR7162, MIR938, MTPAP, SVIL
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3962756
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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