A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18159542



Internal ID20726582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74524469..74527586hg38UCSC Ensembl
chr7:73938799..73941916hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg383118
hg193118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6612243
Supporting Variants
Samples
Known GenesGTF2IRD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18159542
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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