A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010564



Internal ID18753095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16690571..16949734hg38UCSC Ensembl
Innerchr1:17017066..17276229hg19UCSC Ensembl
Innerchr1:16889653..17148816hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38259164
hg19259164
hg18259164
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv78n100
Supporting Variantsnssv3470272
Samples
Known GenesCROCC, ESPNP, LOC729574, MIR3675, MST1L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010564
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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