A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525226



Internal ID15452519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:37723169..37762544hg38UCSC Ensembl
Innerchr1:38188841..38228216hg19UCSC Ensembl
Innerchr1:37961428..38000803hg18UCSC Ensembl
Innerchr1:37857934..37897309hg17UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3839376
hg1939376
hg1839376
hg1739376
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701315
Samples
Known GenesEPHA10
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525226
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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