A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001770



Internal ID19090987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:14779561..14822675hg38UCSC Ensembl
Innerchr1:15106057..15149171hg19UCSC Ensembl
Innerchr1:14978644..15021758hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3843115
hg1943115
hg1843115
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3481126
Samples
Known GenesKAZN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1001770
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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