A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3576963



Internal ID18528558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:11181393..11265120hg38UCSC Ensembl
Innerchr2:11321519..11405246hg19UCSC Ensembl
Innerchr2:11238970..11322697hg18UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3883728
hg1983728
hg1883728
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1013570
Supporting Variants
Samples
Known GenesROCK2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3576963
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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