A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3992350



Internal ID18899873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:137922370..137922440hg38UCSC Ensembl
Outerchr7:137607116..137607186hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1124271
Supporting Variants
SamplesKWS2
Known GenesCREB3L2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3992350
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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