A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702564



Internal ID15092530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:206962646..206970169hg38UCSC Ensembl
Innerchr1:207135991..207143514hg19UCSC Ensembl
Innerchr1:205202614..205210137hg18UCSC Ensembl
Innerchr1:203524386..203531909hg17UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg387524
hg197524
hg187524
hg177524
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526285
Supporting Variants
Samples
Known GenesFCAMR
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702564
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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