A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18153729



Internal ID20720769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:36366773..36370069hg38UCSC Ensembl
chr7:36406382..36409678hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg383297
hg193297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6603038
Supporting Variants
Samples
Known GenesKIAA0895
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18153729
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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