A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997284



Internal ID19156822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:77006300..77076072hg38UCSC Ensembl
Innerchr2:77233426..77303198hg19UCSC Ensembl
Innerchr2:77086934..77156706hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3869773
hg1969773
hg1869773
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3582055
Samples
Known GenesLRRTM4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv997284
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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