A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18156987



Internal ID20724027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:21697244..21768889hg38UCSC Ensembl
chr7:21736862..21808507hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3871646
hg1971646
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6614139
Supporting Variants
Samples
Known GenesDNAH11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18156987
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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