A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977382



Internal ID18265902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:27869847..27907414hg38UCSC Ensembl
Innerchr13:28443984..28481551hg19UCSC Ensembl
Innerchr13:27341984..27379551hg18UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg3837568
hg1937568
hg1837568
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2759305
SamplesHGDP00542
Known GenesPDX1-AS1
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977382
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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