A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3970972



Internal ID19214200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:64200072..64200134hg38UCSC Ensembl
Outerchr15:64492271..64492333hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1131196
Supporting Variants
SamplesKWS1
Known GenesCSNK1G1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3970972
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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