A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141571



Internal ID340768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74807439..74813139hg38UCSC Ensembl
chr7:74221777..74227672hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg385701
hg195896
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17001011
Samples
Known GenesGTF2IRD2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141571
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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