A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3997337



Internal ID19193035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:92214817..92219618hg38UCSC Ensembl
Outerchr9:94977099..94981900hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg384802
hg194802
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1145974
Supporting Variants
SamplesKWB1
Known GenesIARS
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3997337
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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