A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3982154



Internal ID18862586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:83922659..83923270hg38UCSC Ensembl
Outerchr1:84388342..84388953hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38612
hg19612
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1119700
Supporting Variants
SamplesKWS1
Known GenesTTLL7
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3982154
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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