A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18154565



Internal ID20721605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:43542972..43544905hg38UCSC Ensembl
chr7:43582571..43584504hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg381934
hg191934
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6616836
Supporting Variants
Samples
Known GenesHECW1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18154565
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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