A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13707657



Internal ID21229455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:70221381..70221381hg38UCSC Ensembl
chr9:72836297..72836297hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2819349
Supporting Variants
Samples
Known GenesMAMDC2, SMC5-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13707657
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.875


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