A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3962751



Internal ID18872794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:7035377..7053992hg38UCSC Ensembl
Outerchr19:7035388..7054003hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3818616
hg1918616
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1129318
Supporting Variants
SamplesKWS1
Known GenesMBD3L2, MBD3L4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3962751
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