A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3990169



Internal ID19230784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:129177221..129177721hg38UCSC Ensembl
Outerchr9:131939500..131940000hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1137668
Supporting Variants
SamplesKWS2
Known GenesIER5L
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3990169
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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