A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv676369



Internal ID15413021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:229236366..229237877hg38UCSC Ensembl
Innerchr1:229372113..229373624hg19UCSC Ensembl
Innerchr1:227438736..227440247hg18UCSC Ensembl
Innerchr1:225678848..225680359hg17UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg381512
hg191512
hg181512
hg171512
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516336
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv676369
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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