A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3719446



Internal ID19017727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:45674042..45699371hg38UCSC Ensembl
Innerchr17:43751408..43776737hg19UCSC Ensembl
Innerchr17:41107191..41132520hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3825330
hg1925330
hg1825330
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056484
Supporting Variants
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)nssv3719446
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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