A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3957822



Internal ID18859456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:28663036..28663102hg38UCSC Ensembl
Outerchr7:28702653..28702719hg19UCSC Ensembl
Cytoband7p15.1
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1117704
Supporting Variants
SamplesKWS1
Known GenesCREB5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3957822
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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