A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3957881



Internal ID19213172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:104954519..104954584hg38UCSC Ensembl
Outerchr7:104594966..104595031hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1117748
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3957881
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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