A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155178



Internal ID22085683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:51973538..51981087hg38UCSC Ensembl
Outerchr15:51970414..51983058hg38UCSC Ensembl
Innerchr15:52265735..52273284hg19UCSC Ensembl
Outerchr15:52262611..52275255hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3812645
hg1912645
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4011085, nssv4011084
Samples
Known GenesLEO1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155178
Frequency
Sample Size131
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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