A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523131



Internal ID15103738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:178011924..178031386hg38UCSC Ensembl
Innerchr1:177981059..178000521hg19UCSC Ensembl
Innerchr1:176247682..176267144hg18UCSC Ensembl
Innerchr1:174712716..174732178hg17UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg3819463
hg1919463
hg1819463
hg1719463
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698835
Samples
Known GenesLOC730102
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523131
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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