A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705069



Internal ID15441721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:106034370..106110385hg38UCSC Ensembl
InnerchrX:105278361..105354377hg19UCSC Ensembl
InnerchrX:105165017..105241033hg18UCSC Ensembl
InnerchrX:105084506..105160522hg17UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg3876016
hg1976017
hg1876017
hg1776017
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528467
Supporting Variants
Samples
Known GenesSERPINA7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705069
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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