A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423929



Internal ID21081482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:157116114..157127752hg38UCSC Ensembl
chr7:156908808..156920446hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3811639
hg1911639
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18151500
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423929
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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