A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606425



Internal ID16393834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:25036493..25061858hg38UCSC Ensembl
Innerchr7:25076112..25101477hg19UCSC Ensembl
Innerchr7:25042637..25068002hg18UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg3825366
hg1925366
hg1825366
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1154921
SamplesHGDP00163
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606425
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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