A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2761726



Internal ID17422100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:54324475..54331618hg38UCSC Ensembl
Innerchr18:51850845..51857988hg19UCSC Ensembl
Innerchr18:50104843..50111986hg18UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg387144
hg197144
hg187144
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv962973
Supporting Variants
SamplesHGDP00542
Known GenesSTARD6
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2761726
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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