A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705119



Internal ID15095085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:58479909..58515110hg38UCSC Ensembl
Innerchr16:58513813..58549014hg19UCSC Ensembl
Innerchr16:57071314..57106515hg18UCSC Ensembl
Innerchr16:57071314..57106515hg17UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3835202
hg1935202
hg1835202
hg1735202
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528512
Supporting Variants
Samples
Known GenesNDRG4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705119
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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