A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3005526



Internal ID17298478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:64340967..64341309hg38UCSC Ensembl
Outerchr15:64633166..64633508hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38343
hg19343
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv957993
Supporting Variants
SamplesBILGI_BIOE
Known GenesCSNK1G1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3005526
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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