A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1089429



Internal ID15595929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:88039690..88043355hg38UCSC Ensembl
Innerchr7:87669005..87672670hg19UCSC Ensembl
Innerchr7:87506941..87510606hg18UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg383666
hg193666
hg183666
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607737
Supporting Variants
Samples
Known GenesADAM22
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1089429
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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