A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17001629



Internal ID68688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:112214273..112253606hg38UCSC Ensembl
chr7:111854328..111893661hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3839334
hg1939334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5493457
Supporting Variants
Samples
Known GenesZNF277
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17001629
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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