A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3963031



Internal ID19205787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:56422036..56422342hg38UCSC Ensembl
Outerchr1:56887708..56888014hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1120609
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3963031
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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