A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2759305



Internal ID17419156
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 Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv977382
Supporting Variants
SamplesHGDP00542
Known GenesPDX1-AS1
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2759305
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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