A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2810977



Internal ID21256315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:43947985..43947985hg38UCSC Ensembl
chr4:43950002..43950002hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13694548
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2810977
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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