A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17501255



Internal ID22559193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:131020171..131021920hg38UCSC Ensembl
chr7:130704930..130706679hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg381750
hg191750
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5863002
Supporting Variants
Samples
Known GenesLINC-PINT
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17501255
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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