A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026656



Internal ID19115874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:56740039..56940122hg38UCSC Ensembl
Innerchr7:56807732..57007829hg19UCSC Ensembl
Innerchr7:56775226..57011771hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg38200084
hg19200098
hg18236546
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3661462
Samples
Known GenesLOC100130849
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026656
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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