A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020251



Internal ID18762787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:6269897..6340310hg38UCSC Ensembl
Innerchr7:6309528..6379941hg19UCSC Ensembl
Innerchr7:6276053..6346466hg18UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3870414
hg1970414
hg1870414
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3752808
Samples
Known GenesCYTH3, FAM220A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020251
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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