A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3985128



Internal ID19223139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:39374581..39529681hg38UCSC Ensembl
Outerchr8:39232100..39387200hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38155101
hg19155101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1126852
Supporting Variants
SamplesKWS1
Known GenesADAM3A, ADAM5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3985128
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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