A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1077807



Internal ID15584307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:886312..889882hg38UCSC Ensembl
Innerchr7:925949..929519hg19UCSC Ensembl
Innerchr7:892475..896045hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg383571
hg193571
hg183571
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605698
Supporting Variants
Samples
Known GenesGET4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1077807
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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