A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17504508



Internal ID22562451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:141577572..141583810hg38UCSC Ensembl
chr7:141277372..141283610hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg386239
hg196239
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5847642
Supporting Variants
Samples
Known GenesAGK
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17504508
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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