A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981828



Internal ID18617024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:51956559..51965349hg38UCSC Ensembl
Innerchr7:52024255..52033045hg19UCSC Ensembl
Innerchr7:51991749..52000539hg18UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg388791
hg198791
hg188791
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2760526
SamplesHGDP01029
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv981828
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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