A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17434486



Internal ID22492356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140470333..140470467hg38UCSC Ensembl
chr7:140170133..140170267hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5920742
Supporting Variants
Samples
Known GenesMKRN1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17434486
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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