A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526779



Internal ID15454072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:205745264..205750342hg38UCSC Ensembl
Innerchr2:206609988..206615066hg19UCSC Ensembl
Innerchr2:206318233..206323311hg18UCSC Ensembl
Innerchr2:206435494..206440572hg17UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg385079
hg195079
hg185079
hg175079
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703131
Samples
Known GenesNRP2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526779
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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