A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18150785



Internal ID20717825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:141862204..141886080hg38UCSC Ensembl
chr7:141562004..141585880hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3823877
hg1923877
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6425443
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18150785
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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