A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3956771



Internal ID19210567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:139648870..139648931hg38UCSC Ensembl
Outerchr4:140570024..140570085hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1117125
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3956771
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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