A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv677714



Internal ID15067680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:227850423..228109044hg38UCSC Ensembl
Innerchr1:228038124..228296745hg19UCSC Ensembl
Innerchr1:226104747..226363368hg18UCSC Ensembl
Innerchr1:224344859..224603480hg17UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg38258622
hg19258622
hg18258622
hg17258622
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516409
Supporting Variants
Samples
Known GenesARF1, C1orf35, MIR3620, MIR5008, MRPL55, WNT3A, WNT9A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv677714
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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