A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606676



Internal ID16394085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:39503235..39512001hg38UCSC Ensembl
Innerchr7:39542834..39551600hg19UCSC Ensembl
Innerchr7:39509359..39518125hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg388767
hg198767
hg188767
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11283n54
Supporting Variantsnssv1082843
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606676
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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