A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4011102



Internal ID22072733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:59684582..59755084hg38UCSC Ensembl
Outerchr15:59682367..59761114hg38UCSC Ensembl
Innerchr15:59976781..60047283hg19UCSC Ensembl
Outerchr15:59974566..60053313hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3878748
hg1978748
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155185
Supporting Variants
Samples
Known GenesBNIP2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4011102
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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