A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18154572



Internal ID20721612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:43642412..43644789hg38UCSC Ensembl
chr7:43682011..43684388hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg382378
hg192378
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6606234
Supporting Variants
Samples
Known GenesCOA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18154572
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00023


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