A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3969324



Internal ID19245552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:136033454..136056554hg38UCSC Ensembl
Outerchr9:138925300..138948400hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3823101
hg1923101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1133749
Supporting Variants
SamplesKWS2
Known GenesNACC2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3969324
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