A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155170



Internal ID22085675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:43622551..43703690hg38UCSC Ensembl
Outerchr15:43604064..43719842hg38UCSC Ensembl
Innerchr15:43914749..43995888hg19UCSC Ensembl
Outerchr15:43896262..44012040hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg38115779
hg19115779
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4011063, nssv4011064
Samples
Known GenesCATSPER2, CKMT1A, STRC
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155170
Frequency
Sample Size131
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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