A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524709



Internal ID15105316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:33266591..33271825hg38UCSC Ensembl
Innerchr1:33732192..33737426hg19UCSC Ensembl
Innerchr1:33504779..33510013hg18UCSC Ensembl
Innerchr1:33401285..33406519hg17UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg385235
hg195235
hg185235
hg175235
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700693
Samples
Known GenesZNF362
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524709
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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