A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3980263



Internal ID19215187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:38076702..38076809hg38UCSC Ensembl
Outerchr9:38076699..38076806hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1118061
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3980263
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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