A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14251401



Internal ID21302685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:43622551..43703690hg38UCSC Ensembl
Outerchr15:43604064..43719842hg38UCSC Ensembl
Innerchr15:43914749..43995888hg19UCSC Ensembl
Outerchr15:43896262..44012040hg19UCSC Ensembl
Innerchr15:41702041..41783180hg18UCSC Ensembl
Outerchr15:41683554..41799332hg18UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg38115779
hg19115779
hg18115779
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169433
Supporting Variants
SamplesMLY_16
Known GenesCATSPER2, CKMT1A, STRC
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14251401
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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