A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3976951



Internal ID19240194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:127725426..127725481hg38UCSC Ensembl
Outerchr9:130487705..130487760hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1137506
Supporting Variants
SamplesKWS2
Known GenesTTC16
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3976951
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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