A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6604422



Internal ID20977493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74577249..74588274hg38UCSC Ensembl
chr7:73991579..74002603hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3811026
hg1911025
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18159549
Samples
Known GenesGTF2IRD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6604422
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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