A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1078372



Internal ID15931558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:1881726..1979235hg38UCSC Ensembl
Innerchr7:1921362..2018870hg19UCSC Ensembl
Innerchr7:1887888..1985396hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3897510
hg1997509
hg1897509
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605834
Supporting Variants
Samples
Known GenesMAD1L1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1078372
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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