A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609935



Internal ID20983006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:43651579..43662327hg38UCSC Ensembl
chr7:43691178..43701926hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg3810749
hg1910749
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154573
Samples
Known GenesCOA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609935
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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