A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702519



Internal ID15439171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:21292826..21315952hg38UCSC Ensembl
Innerchr16:21304147..21327273hg19UCSC Ensembl
Innerchr16:21211648..21234774hg18UCSC Ensembl
Innerchr16:21211648..21234774hg17UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg3823127
hg1923127
hg1823127
hg1723127
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526247
Supporting Variants
Samples
Known GenesCRYM, CRYM-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702519
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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