A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3974525



Internal ID19204820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:39360072..39361376hg38UCSC Ensembl
Outerchr13:39934209..39935513hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg381305
hg191305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1114617
Supporting Variants
SamplesKWS1
Known GenesLHFP
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3974525
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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