A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3966632



Internal ID19235791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:54406127..54406527hg38UCSC Ensembl
Outerchr1:54871800..54872200hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38401
hg19401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1112533
Supporting Variants
SamplesKWS2
Known GenesSSBP3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3966632
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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