A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981827



Internal ID18617023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:37586264..37596784hg38UCSC Ensembl
Innerchr7:37625867..37636387hg19UCSC Ensembl
Innerchr7:37592392..37602912hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3810521
hg1910521
hg1810521
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2756718
SamplesHGDP00456
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv981827
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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