A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv971192



Internal ID18259726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:20340443..20342679hg38UCSC Ensembl
Innerchr7:20380066..20382302hg19UCSC Ensembl
Innerchr7:20346591..20348827hg18UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg382237
hg192237
hg182237
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2759607
SamplesHGDP00456
Known GenesITGB8
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv971192
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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