A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997255



Internal ID19156793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:56815888..57203574hg38UCSC Ensembl
Innerchr2:57043023..57430709hg19UCSC Ensembl
Innerchr2:56896527..57284213hg18UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg38387687
hg19387687
hg18387687
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3576693
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv997255
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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