A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv971550



Internal ID18260081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:22671337..22682562hg38UCSC Ensembl
Innerchr7:22710956..22722181hg19UCSC Ensembl
Innerchr7:22677481..22688706hg18UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3811226
hg1911226
hg1811226
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2763139
SamplesHGDP00456
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv971550
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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