A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521525



Internal ID15102132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:6319547..6327724hg38UCSC Ensembl
Innerchr1:6379607..6387784hg19UCSC Ensembl
Innerchr1:6302194..6310371hg18UCSC Ensembl
Innerchr1:6313873..6322050hg17UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg388178
hg198178
hg188178
hg178178
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698142
Samples
Known GenesACOT7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521525
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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