A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17445769



Internal ID22503639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:36337098..36337098hg38UCSC Ensembl
chr7:36376707..36376707hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg38223
hg19223
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5958774
Supporting Variants
Samples
Known GenesKIAA0895
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17445769
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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