A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1078355



Internal ID15931541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:1415102..1440650hg38UCSC Ensembl
Innerchr7:1454738..1480286hg19UCSC Ensembl
Innerchr7:1421264..1446812hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3825549
hg1925549
hg1825549
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605817
Supporting Variants
Samples
Known GenesMICALL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1078355
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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