A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020577



Internal ID19109796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:8844447..9116407hg38UCSC Ensembl
Innerchr7:8884077..9156037hg19UCSC Ensembl
Innerchr7:8850602..9122562hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38271961
hg19271961
hg18271961
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6259n100
Supporting Variantsnssv3642857
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)nsv1020577
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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