A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156700



Internal ID22087101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:91402420..91411412hg38UCSC Ensembl
Outerchr7:91402190..91417678hg38UCSC Ensembl
Innerchr7:91031735..91040727hg19UCSC Ensembl
Outerchr7:91031505..91046993hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3815489
hg1915489
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv266n97
Supporting Variantsnssv4022196, nssv4022193, nssv4022191, nssv4022189, nssv4022188, nssv4022185, nssv4022197, nssv4022195, nssv4022194, nssv4022192, nssv4022190, nssv4022186
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156700
Frequency
Sample Size131
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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