A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17434789



Internal ID22492659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:65186338..65692583hg38UCSC Ensembl
chr7:64646716..65157550hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38506246
hg19510835
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5918237
Supporting Variants
Samples
Known GenesINTS4L2, LOC441242, ZNF92
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17434789
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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