A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064736



Internal ID19153955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:45668910..45699947hg38UCSC Ensembl
Innerchr17:43746276..43777313hg19UCSC Ensembl
Innerchr17:41102059..41133096hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3831038
hg1931038
hg1831038
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3177n100
Supporting Variantsnssv3719445
Samples
Known GenesCRHR1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064736
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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