A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702177



Internal ID15092143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:158931337..158932554hg38UCSC Ensembl
Innerchr1:158901127..158902344hg19UCSC Ensembl
Innerchr1:157167751..157168968hg18UCSC Ensembl
Innerchr1:155714200..155715417hg17UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg381218
hg191218
hg181218
hg171218
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525964
Supporting Variants
Samples
Known GenesPYHIN1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702177
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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