A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156648



Internal ID22087049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:16309218..16362489hg38UCSC Ensembl
Outerchr7:16309138..16363297hg38UCSC Ensembl
Innerchr7:16348843..16402114hg19UCSC Ensembl
Outerchr7:16348763..16402922hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3854160
hg1954160
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4021057, nssv4021058
Samples
Known GenesISPD
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156648
Frequency
Sample Size131
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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