A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698798



Internal ID15435450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:124476053..124483250hg38UCSC Ensembl
Innerchr9:127238332..127245529hg19UCSC Ensembl
Innerchr9:126278153..126285350hg18UCSC Ensembl
Innerchr9:124317886..124325083hg17UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg387198
hg197198
hg187198
hg177198
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517372
Supporting Variants
Samples
Known GenesNR5A1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698798
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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