A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18158609



Internal ID20725649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:65063205..65752770hg38UCSC Ensembl
chr7:64523583..65217757hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38689566
hg19694175
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6610802
Supporting Variants
Samples
Known GenesCCT6P1, CCT6P3, INTS4L2, LOC441242, ZNF92
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18158609
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00382


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