A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006617



Internal ID19095834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25256340..25320483hg38UCSC Ensembl
Innerchr1:25582831..25646974hg19UCSC Ensembl
Innerchr1:25455418..25519561hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3864144
hg1964144
hg1864144
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv138n100
Supporting Variantsnssv3475959, nssv3480081
Samples
Known GenesRHD
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1006617
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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