A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3976922



Internal ID18888369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:86081781..86081846hg38UCSC Ensembl
Outerchr9:88696696..88696761hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1137475
Supporting Variants
SamplesKWS2
Known GenesGOLM1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3976922
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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