A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997768



Internal ID19157305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:72117692..72199585hg38UCSC Ensembl
Innerchr1:72583375..72665268hg19UCSC Ensembl
Innerchr1:72355963..72437856hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3881894
hg1981894
hg1881894
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3464438
Samples
Known GenesNEGR1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv997768
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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