A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5965631



Internal ID22740567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:75140530..75140530hg38UCSC Ensembl
chrX:74360365..74360365hg19UCSC Ensembl
CytobandXq13.3
Allele length
AssemblyAllele length
hg38171
hg19171
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17462961
Samples
Known GenesABCB7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5965631
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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