A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5909702



Internal ID22684912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:75704496..75704824hg38UCSC Ensembl
chr7:75333814..75334142hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38329
hg19329
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17434020
Samples
Known GenesHIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5909702
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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