A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606036



Internal ID16046759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:7233928..7304278hg38UCSC Ensembl
Innerchr7:7273559..7343909hg19UCSC Ensembl
Innerchr7:7240084..7310434hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3870351
hg1970351
hg1870351
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1078875
Samples
Known GenesC1GALT1, LOC101927354
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606036
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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