A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv706092



Internal ID15096058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:154095720..154144396hg38UCSC Ensembl
Innerchr1:154068196..154116872hg19UCSC Ensembl
Innerchr1:152334820..152383496hg18UCSC Ensembl
Innerchr1:150881269..150929945hg17UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3848677
hg1948677
hg1848677
hg1748677
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520398
Supporting Variants
Samples
Known GenesNUP210L
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv706092
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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