A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18156432



Internal ID20723472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:37680154..37685258hg38UCSC Ensembl
chr7:37719757..37724861hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg385105
hg195105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6610034
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18156432
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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