A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3993136



Internal ID19243400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:64371982..64462182hg38UCSC Ensembl
Outerchr9:69384400..69474600hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3890201
hg1990201
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1141631
Supporting Variants
SamplesKWS2
Known GenesANKRD20A4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3993136
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