A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3977979



Internal ID19242947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:6894537..6894597hg38UCSC Ensembl
Outerchr10:6936499..6936559hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1125174
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3977979
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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