A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17433554



Internal ID22491424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140172381..140173890hg38UCSC Ensembl
chr7:139872181..139873690hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg381510
hg191510
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5921340
Supporting Variants
Samples
Known GenesKDM7A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17433554
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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