A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3969300



Internal ID19241899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:39363827..39379815hg38UCSC Ensembl
Outerchr9:65485400..65501500hg19UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3815989
hg1916101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1133724
Supporting Variants
SamplesKWS2
Known GenesFAM74A2, FAM74A4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3969300
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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