A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv673990



Internal ID15063956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70660097..70806587hg38UCSC Ensembl
Innerchr16:70694000..70840490hg19UCSC Ensembl
Innerchr16:69251501..69397991hg18UCSC Ensembl
Innerchr16:69251501..69397991hg17UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38146491
hg19146491
hg18146491
hg17146491
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517391
Supporting Variants
Samples
Known GenesIL34, MTSS1L, VAC14, VAC14-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv673990
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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