A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3962746



Internal ID18877384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:7035386..7054271hg38UCSC Ensembl
Outerchr19:7035397..7054282hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3818886
hg1918886
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1129313
Supporting Variants
SamplesKWS1
Known GenesMBD3L2, MBD3L4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3962746
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer