A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3978632



Internal ID18891133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:13063131..13063427hg38UCSC Ensembl
Outerchr10:13105131..13105427hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1116451
Supporting Variants
SamplesKWS2
Known GenesCCDC3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3978632
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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